Antisense modulation of PTP1B expression

Abstract

Compounds, compositions and methods are provided for modulating the expression of PTP1B. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding PTP1B. Methods of using these compounds for modulation of PTP1B expression and for treatment of diseases associated with expression of PTP1B are provided.

Parent Case Text

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 12/046,421, filed Mar. 11, 2008, allowed May 5, 2011, which is a continuation of U.S. application Ser. No. 11/194,776, filed Aug. 1, 2005, which is a continuation of PCT Application No. PCT/US04/002003, filed Feb. 6, 2004, which is a continuation-in-part of U.S. application Ser. No. 10/360,510 filed Feb. 7, 2003, which is a continuation-in-part of U.S. application Ser. No. 09/854,883, each of which is incorporated herein by reference in its entirety. U.S. application Ser. No. 12/046,721 is also a continuation-in-part of U.S. application Ser. No. 11/008,747, filed Dec. 9, 2004, which is a continuation of U.S. application Ser. No. 09/854,883, filed May 14, 2001, each of which is incorporated herein by reference in its entirety.

Description

SEQUENCE LISTING

The present application is being filed along with a Sequence Listing in electronic format. The Sequence Listing is provided as a file entitled BIOL0001 USC4SEQ.txt, created on Jul. 6, 2011 which is 188 Kb in size. The information in the electronic format of the sequence listing is incorporated herein by reference in its entirety.

BACKGROUND OF THE INVENTION

The process of phosphorylation, defined as the attachment of a phosphate moiety to a biological molecule through the action of enzymes called kinases, represents one course by which intracellular signals are propagated resulting finally in a cellular response. Within the cell, proteins can be phosphorylated on serine, threonine or tyrosine residues and the extent of phosphorylation is regulated by the opposing action of phosphatases, which remove the phosphate moieties. While the majority of protein phosphorylation within the cell is on serine and threonine residues, tyrosine phosphorylation is modulated to the greatest extent during oncogenic transformation and growth factor stimulation (Zhang, Crit. Rev. Biochem. Mol. Biol., 1998, 33, 1-52).

Because phosphorylation is such a ubiquitous process within cells and because cellular phenotypes are largely influenced by the activity of these pathways, it is currently believed that a number of disease states and/or disorders are a result of either aberrant activation of, or functional mutations in, kinases and phosphatases. Consequently, considerable attention has been devoted recently to the characterization of tyrosine kinases and tyrosine phosphatases.

PTP1B (also known as protein phosphatase 1B and PTPN1) is an endoplasmic reticulum (ER)-associated enzyme originally isolated as the major protein tyrosine phosphatase of the human placenta (Tonks et al., J. Biol. Chem., 1988, 263, 6731-6737; Tonks et al., J. Biol. Chem., 1988, 263, 6722-6730).

An essential regulatory role in signaling mediated by the insulin receptor has been established for PTP1B. PTP1B interacts with and dephosphorylates the activated insulin receptor both in vitro and in intact cells resulting in the downregulation of the signaling pathway (Goldstein et al., Mol. Cell. Biochem., 1998, 182, 91-99; Seely et al., Diabetes, 1996, 45, 1379-1385). In addition, PTP1B modulates the mitogenic actions of insulin (Goldstein et al., Mol. Cell. Biochem., 1998, 182, 91-99). In rat adipose cells overexpressing PTP1B, the translocation of the GLUT4 glucose transporter was inhibited, implicating PTP1B as a negative regulator of glucose transport as well (Chen et al., J. Biol. Chem., 1997, 272, 8026-8031).

Mouse knockout models lacking the PTP1B gene also point toward the negative regulation of insulin signaling by PTP1B. Mice harboring a disrupted PTP1B gene showed increased insulin sensitivity, increased phosphorylation of the insulin receptor and when placed on a high-fat diet, PTP1B-/- mice were resistant to weight gain and remained insulin sensitive (Elchebly et al., Science, 1999, 283, 1544-1548). These studies clearly establish PTP1B as a therapeutic target in the treatment of diabetes and obesity.

PTP1B, which is differentially regulated during the cell cycle (Schievella et al., Cell. Growth Differ., 1993, 4, 239-246), is expressed in insulin sensitive tissues as two different isoforms that arise from alternate splicing of the pre-mRNA (Shifrin and Neel, J. Biol. Chem., 1993, 268, 25376-25384). It was recently demonstrated that the ratio of the alternatively spliced products is affected by growth factors such as insulin and differs in various tissues examined (Sell and Reese, Mol. Genet. Metab., 1999, 66, 189-192). In these studies it was also found that the levels of the variants correlated with the plasma insulin concentration and percentage body fat and may therefore be used as a biomarker for patients with chronic hyperinsulinemia or type 2 diabetes.

Liu and Chernoff have shown that PTP1B binds to and serves as a substrate for the epidermal growth factor receptor (EGFR) (Liu and Chernoff, Biochem. J., 1997, 327, 139-145). Furthermore, in A431 human epidermoid carcinoma cells, PT1B was found to be inactivated by the presence of H.sub.2O.sub.2 generated by the addition of EGF. These studies indicate that PTP1B can be negatively regulated by the oxidation state of the cell, which is often deregulated during tumorigenesis (Lee et al., J. Biol. Chem., 1998, 273, 15366-15372).

Overexpression of PTP1B has been demonstrated in malignant ovarian cancers and this correlation was accompanied by a concomitant increase in the expression of the associated growth factor receptor (Wiener et al., Am. J. Obstet. Gynecol., 1994, 170, 1177-1183).

PTP1B has been shown to suppress transformation in NIH3T3 cells induced by the neu oncogene (Brown-Shimer et al., Cancer Res., 1992, 52, 478-482), as well as in rat 3Y1 fibroblasts induced by v-srk, v-src, and v-ras (Liu et al., Mol. Cell. Biol., 1998, 18, 250-259) and rat-1 fibroblasts induced by bcr-abl (LaMontagne et al., Proc. Natl. Acad. Sci. U.S.A., 1998, 95, 14094-14099). It has also been shown that PTP1B promotes differentiation of K562 cells, a chronic myelogenous leukemia cell line, in a similar manner as does an inhibitor of the bcr-abl oncoprotein. These studies describe the possible role of PTP1B in controlling the pathogenesis of chronic myeloid leukemia (LaMontagne et al., Proc. Natl. Acad. Sci. U.S.A., 1998, 95, 14094-14099).

PTP1B negatively regulates integrin signaling by interacting with one or more adhesion-dependent signaling components and repressing integrin-mediated MAP kinase activation (Liu et al., Curr. Biol., 1998, 8, 173-176). Other studies designed to study integrin signaling, using a catalytically inactive form of PTP1B, have shown that PTP1B regulates cadherin-mediated cell adhesion (Balsamo et al., J. Cell. Biol., 1998, 143, 523-532) as well as cell spreading, focal adhesion and stress fiber formation and tyrosine phosphorylation (Arregui et al., J. Cell. Biol., 1998, 143, 861-873).

Currently, therapeutic agents designed to inhibit the synthesis or action of PTP1B include small molecules (Ham et al., Bioorg. Med. Chem. Lett., 1999, 9, 185-186; Skorey et al., J. Biol. Chem., 1997, 272, 22472-22480; Taing et al., Biochemistry, 1999, 38, 3793-3803; Taylor et al., Bioorg. Med. Chem., 1998, 6, 1457-1468; Wang et al., Bioorg. Med. Chem. Lett., 1998, 8, 345-350; Wang et al., Biochem. Pharmacol., 1997, 54, 703-711; Yao et al., Bioorg. Med. Chem., 1998, 6, 1799-1810) and peptides (Chen et al., Biochemistry, 1999, 38, 384-389; Desmarais et al., Arch. Biochem. Biophys., 1998, 354, 225-231; Roller et al., Bioorg. Med. Chem. Lett., 1998, 8, 2149-2150). In addition, disclosed in the PCT publication WO 97/32595 (Olefsky, 1997) are phosphopeptides and antibodies that inhibit the association of PTP1B with the activated insulin receptor for the treatment of disorders associated with insulin resistance. Antisense nucleotides against PTP1B are also generally disclosed.

There remains a long felt need for additional agents capable of effectively inhibiting PTP1B function.

SUMMARY OF THE INVENTION

Contemplated herein are compounds comprising a sense region and an antisense region, said antisense region comprising an antisense compound targeted to PTP1b. Also contemplated are compounds comprising a sense region and an antisense region, said antisense region comprising a sequence exemplified herein. In a preferred embodiment, the compounds specifically hybridize with a nucleic acid molecule encoding PTP1B and inhibit the expression of PTP1B. In some embodiments, the antisense region and the sense region are separate molecules. In some embodiments, the antisense region and the sense region are part of a single molecule.

Further contemplated are antisense regions comprising a stretch of at least eight (8) consecutive nucleobases of sequences described herein, preferably of SEQ ID NO: 18, 19, 20, 21, 22, 23, 24, 26, 27, 29, 30, 32, 33, 35, 36, 38, 39, 40, 42, 45, 46, 47, 48, 49, 50, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 69, 70, 72, 73, 75, 78, 79, 80, 81, 83, 84, 86, 87, 89, 90, 92, 93, 94, 95, 96, 97, 99, 100, 101, 102, 103, 104, 106, 107, 108, 109, 110, 112, 113, 114, 115, 117, 120, 121, 122, 123, 124, 126, 127, 128, 130, 131, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 144, 145, 146, 147, 148, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 191, 193, 195, 196, 198, 201, 202, 204, 205, 206, 211, 215, 217, 219, 223, 225, 226, 228, 229, 230, 232, 233, 235, 236, 237, 239, 240, 244, 245, 247, 248, 249, 250, 251, 252, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 267, 268, 269, 271, 275, 276, 277, 278, 279, 281, 282, 283, 288, 290, 291, 292, 294, 296, 297, 298, 299, 300, 302, 303, 307, 310, 311, 313, 315, 317, 318, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 337, 340, 341, 342, 343, 344, 345, 347, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 360, 361, 362, 363, 364, 365, 366, 368, 369, 371, 372, 373, 374, 375, 377, 378, 380, 381, 384, 385, 386, 387, 388, 389, 390, 391, 392, 393, 394, 395, 396, 397, or 398 wherein said compound specifically hybridizes with said nucleic acid molecule encoding PTP1B and inhibits the expression of PTP1B.

Further provided are compounds 8 to 50 nucleobases in length targeted to a nucleic acid molecule encoding PTP1B, wherein said compound comprises a sense region and an antisense region, said antisense region comprising a stretch of at least eight (8) consecutive nucleobases of SEQ ID NO: 390, 391, 392, 393, 394, 395, 396, 397, or 398 or comprising a stretch of at least eight (8) consecutive nucleobases of nucleobases 1 to 19 of SEQ ID NO: 390, 391, 392, 393, 394, or 395. In one embodiment, said sense region comprises a sequence complementary to the antisense region selected from sequences comprising a stretch of at least eight (8) consecutive nucleobases of SEQ ID NO: 403, 404, 405, 406, 407, 408, 409, 410, or 411 or comprising a stretch of at least eight (8) consecutive nucleobases of nucleobases 1 to 19 of SEQ ID NO: 403, 404, 405, 406, 407, or 408

Further provided are compounds 8 to 50 nucleobases in length targeted to a nucleic acid molecule encoding PTP1B, wherein said compound comprises a sense region and an antisense region, said antisense region comprising a stretch of at least eight (8) consecutive nucleobases of SEQ ID NO: 396, 397, or 398. In some embodiments, said sense region comprises a sequence complementary to said antisense region selected from sequences comprising a stretch of at least eight (8) consecutive nucleobases of SEQ ID NO: 409, 410, or 411.

Another aspect of the present invention are compounds 8 to 50 nucleobases in length targeted to a nucleic acid molecule encoding PTP1B, wherein said compound comprises a sense region and an antisense region, said antisense region comprising a stretch of at least eight (8) consecutive nucleobases of SEQ ID NO: 166.

In some embodiments, the antisense region and/or the sense region further comprise an overhang of two deoxynucleotides.

In some embodiments, the compound comprises at least one modified internucleoside linkage, such as a phosphorothioate linkage, a modified sugar moiety, and/or modified nucleobase. The compounds may be chimeric compounds in some embodiments.

Further contemplated are pharmaceutical compositions comprising the compounds of the invention and a pharmaceutically acceptable carrier, diluent, enhancer or excipient. Also contemplated is a method of inhibiting the expression of PTP1B in cells or tissues comprising contacting said cells or tissues with a compound of the invention so that expression of PTP1B is inhibited.

Another aspect of the present invention is a method of treating an animal having a disease or condition associated with PTP1B comprising administering to said animal a therapeutically or prophylactically effective amount of an antisense compound of the invention so that PTP1B is inhibited. In some embodiments, diseases or conditions include metabolic diseases or conditions. In some embodiments, diseases or conditions include diabetes, obesity, or hyperproliferative disorders including cancer. In some embodiments, the diabetes is Type 2 diabetes.

Other embodiments of the present invention are methods of decreasing blood glucose levels or plasma insulin levels or improving insulin sensitivity in an animal. In some embodiments, the animal is diabetic, hyperinsulinemic, insulin-resistant or obese. Also contemplated herein is the use of a compound of the present invention in the preparation of a medicament for a metabolic disease or condition, wherein said disease or condition is diabetes, including Type 2 diabetes, obesity, or a hyperproliferative condition.

DETAILED DESCRIPTION OF THE INVENTION

The present invention employs oligomeric antisense compounds, particularly oligonucleotides, for use in modulating the function of nucleic acid molecules encoding PTP1B, ultimately modulating the amount of PTP1B produced. This is accomplished by providing antisense compounds which specifically hybridize with one or more nucleic acids encoding PTP1B. As used herein, the terms "target nucleic acid" and "nucleic acid encoding PTP1B" encompass DNA encoding PTP1B, RNA (including pre-mRNA and mRNA) transcribed from such DNA, and also cDNA derived from such RNA. The specific hybridization of an oligomeric compound with its target nucleic acid interferes with the normal function of the nucleic acid. This modulation of function of a target nucleic acid by compounds which specifically hybridize to it is generally referred to as "antisense".

The functions of DNA to be interfered with include replication and transcription. The functions of RNA to be interfered with include all vital functions such as, for example, translocation of the RNA to the site of protein translation, translation of protein from the RNA, splicing of the RNA to yield one or more mRNA species, and catalytic activity which may be engaged in or facilitated by the RNA. The overall effect of such interference with target nucleic acid function is modulation of the expression of PTP1B. In the context of the present invention, "modulation" means either an increase (stimulation) or a decrease (inhibition) in the expression of a gene. In the context of the present invention, inhibition is the preferred form of modulation of gene expression and mRNA is a preferred target.

It is preferred to target specific nucleic acids for antisense. "Targeting" an antisense compound to a particular nucleic acid, in the context of this invention, is a multistep process. The process usually begins with the identification of a nucleic acid sequence whose function is to be modulated. This may be, for example, a cellular gene (or mRNA transcribed from the gene) whose expression is associated with a particular disorder or disease state, or a nucleic acid molecule from an infectious agent. In the present invention, the target is a nucleic acid molecule encoding PTP1B. The targeting process also includes determination of a site or sites within this gene for the antisense interaction to occur such that the desired effect, e.g., detection or modulation of expression of the protein, will result. Within the context of the present invention, a preferred intragenic site is the region encompassing the translation initiation or termination codon of the open reading frame (ORF) of the gene. Since, as is known in the art, the translation initiation codon is typically 5'-AUG (in transcribed mRNA molecules; 5'-ATG in the corresponding DNA molecule), the translation initiation codon is also referred to as the "AUG codon," the "start codon" or the "AUG start codon". A minority of genes has a translation initiation codon having the RNA sequence 5'-GUG, 5'-UUG or 5'-CUG, and 5'-AUA, 5'-ACG and 5'-CUG have been shown to function in vivo. Thus, the terms "translation initiation codon" and "start codon" can encompass many codon sequences, even though the initiator amino acid in each instance is typically methionine (in eukaryotes) or formylmethionine (in prokaryotes). It is also known in the art that eukaryotic and prokaryotic genes may have two or more alternative start codons, any one of which may be preferentially utilized for translation initiation in a particular cell type or tissue, or under a particular set of conditions. In the context of the invention, "start codon" and "translation initiation codon" refer to the codon or codons that are used in vivo to initiate translation of an mRNA molecule transcribed from a gene encoding PTP1B, regardless of the sequence(s) of such codons.

It is also known in the art that a translation termination codon (or "stop codon") of a gene may have one of three sequences, i.e., 5'-UAA, 5'-UAG and 5'-UGA (the corresponding DNA sequences are 5'-TAA, 5'-TAG and 5'-TGA, respectively). The terms "start codon region" and "translation initiation codon region" refer to a portion of such an mRNA or gene that encompasses from about 25 to about 50 contiguous nucleotides in either direction (i.e., 5' or 3') from a translation initiation codon. Similarly, the terms "stop codon region" and "translation termination codon region" refer to a portion of such an mRNA or gene that encompasses from about 25 to about 50 contiguous nucleotides in either direction (i.e., 5' or 3') from a translation termination codon.

The open reading frame (ORF) or "coding region," which is known in the art to refer to the region between the translation initiation codon and the translation termination codon, is also a region which may be targeted effectively. Other target regions include the 5' untranslated region (5'UTR), known in the art to refer to the portion of an mRNA in the 5' direction from the translation initiation codon, and thus including nucleotides between the 5' cap site and the translation initiation codon of an mRNA or corresponding nucleotides on the gene, and the 3' untranslated region (3'UTR), known in the art to refer to the portion of an mRNA in the 3' direction from the translation termination codon, and thus including nucleotides between the translation termination codon and 3' end of an mRNA or corresponding nucleotides on the gene. The 5' cap of an mRNA comprises an N7-methylated guanosine residue joined to the 5'-most residue of the mRNA via a 5'-5' triphosphate linkage. The 5' cap region of an mRNA is considered to include the 5' cap structure itself as well as the first 50 nucleotides adjacent to the cap. The 5' cap region may also be a preferred target region.

Although some eukaryotic mRNA transcripts are directly translated, many contain one or more regions, known as "introns," which are excised from a transcript before it is translated. The remaining (and therefore translated) regions are known as "exons" and are spliced together to form a continuous mRNA sequence. mRNA splice sites, i.e., intron-exon junctions, may also be preferred target regions, and are particularly useful in situations where aberrant splicing is implicated in disease, or where an overproduction of a particular mRNA splice product is implicated in disease. Aberrant fusion junctions due to rearrangements or deletions are also preferred targets. It has also been found that introns can also be effective, and therefore preferred, target regions for antisense compounds targeted, for example, to DNA or pre-mRNA.

Once one or more target sites have been identified, oligonucleotides are chosen which are sufficiently complementary to the target, i.e., hybridize sufficiently well and with sufficient specificity, to give the desired effect.

In the context of this invention, "hybridization" means hydrogen bonding, which may be Watson-Crick, Hoogsteen or reversed Hoogsteen hydrogen bonding, between complementary nucleoside or nucleotide bases. For example, adenine and thymine are complementary nucleobases which pair through the formation of hydrogen bonds. "Complementary," as used herein, refers to the capacity for precise pairing between two nucleotides. For example, if a nucleotide at a certain position of an oligonucleotide is capable of hydrogen bonding with a nucleotide at the same position of a DNA or RNA molecule, then the oligonucleotide and the DNA or RNA are considered to be complementary to each other at that position. The oligonucleotide and the DNA or RNA are complementary to each other when a sufficient number of corresponding positions in each molecule are occupied by nucleotides which can hydrogen bond with each other. Thus, "specifically hybridizable" and "complementary" are terms which are used to indicate a sufficient degree of complementarity or precise pairing such that stable and specific binding occurs between the oligonucleotide and the DNA or RNA target. It is understood in the art that the sequence of an antisense compound need not be 100% complementary to that of its target nucleic acid to be specifically hybridizable. An antisense compound is specifically hybridizable when binding of the compound to the target DNA or RNA molecule interferes with the normal function of the target DNA or RNA to cause a loss of utility, and there is a sufficient degree of complementarity to avoid non-specific binding of the antisense compound to non-target sequences under conditions in which specific binding is desired, i.e., under physiological conditions in the case of in vivo assays or therapeutic treatment, and in the case of in vitro assays, under conditions in which the assays are performed.

The PTP1B inhibitors of the present invention effectively inhibit the activity of the PTP1B protein or inhibit the expression of the PTP1B protein. In one embodiment, the activity or expression of PTP1B is inhibited by about 10%. Preferably, the activity or expression of PTP1B is inhibited by about 30%. More preferably, the activity or expression of PTP1B is inhibited by 50% or more. Thus, the oligomeric antisense compounds modulate expression of PTP1B mRNA by at least 10%, by at least 20%, by at least 25%, by at least 30%, by at least 40%, by at least 50%, by at least 60%, by at least 70%, by at least 75%, by at least 80%, by at least 85%, by at least 90%, by at least 95%, by at least 98%, by at least 99%, or by 100%.

The compounds of the present inventions are inhibitors of PTP1B expression. Thus, the compounds of the present invention are believed to be useful for treating metabolic diseases and conditions, particularly diabetes, obesity, hyperlipidemia or metabolic syndrome X. The compounds of the invention are also believed to be useful for preventing or delaying the onset of metabolic diseases and conditions, particularly diabetes, obesity, hyperlipidemia or metabolic syndrome X. Metabolic syndrome, metabolic syndrome X or simply Syndrome X refers to a cluster of risk factors that include obesity, dyslipidemia, particularly high blood triglycerides, glucose intolerance, high blood sugar and high blood pressure (Scott, C. L., Am. J. Cardiol. 2003 Jul. 3; 92(1A): 35i-42i). Antisense inhibitors of PTP1B have surprisingly been found to be effective for lowering blood glucose, including plasma glucose, and for lowering blood lipids, including serum lipids, particularly serum cholesterol and serum triglycerides. The compounds of the invention are therefore particularly useful in medicaments for the treatment, prevention and delay of onset of type 2 diabetes, high blood glucose and hyperlipidemia.

It is understood in the art that the sequence of an antisense compound need not be 100% complementary to that of its target nucleic acid to be specifically hybridizable. Moreover, an oligonucleotide may hybridize over one or more segments such that intervening or adjacent segments are not involved in the hybridization event (e.g., a loop structure or hairpin structure). It is preferred that the antisense compounds of the present invention comprise at least 70%, or at least 75%, or at least 80%, or at least 85% sequence complementarity to a target region within the target nucleic acid, more preferably that they comprise at least 90% sequence complementarity and even more preferably comprise at least 95% or at least 99% sequence complementarity to the target region within the target nucleic acid sequence to which they are targeted. For example, an antisense compound in which 18 of 20 nucleobases of the antisense compound are complementary to a target region, and would therefore specifically hybridize, would represent 90 percent complementarity. In this example, the remaining noncomplementary nucleobases may be clustered or interspersed with complementary nucleobases and need not be contiguous to each other or to complementary nucleobases. As such, an antisense compound which is 18 nucleobases in length having 4 (four) noncomplementary nucleobases which are flanked by two regions of complete complementarity with the target nucleic acid would have 77.8% overall complementarity with the target nucleic acid and would thus fall within the scope of the present invention.

Percent complementarity of an antisense compound with a region of a target nucleic acid can be determined routinely using BLAST programs (basic local alignment search tools) and PowerBLAST programs known in the art (Altschul et al., J. Mol. Biol., 1990, 215, 403-410; Zhang and Madden, Genome Res., 1997, 7, 649-656).

Percent homology, sequence identity or complementarity, can be determined by, for example, the Gap program (Wisconsin Sequence Analysis Package, Version 8 for Unix, Genetics Computer Group, University Research Park, Madison Wis.), using default settings, which uses the algorithm of Smith and Waterman (Adv. Appl. Math., 1981, 2, 482-489). In some preferred embodiments, homology, sequence identity or complementarity, between the oligomeric and target is between about 50% to about 60%. In some embodiments, homology, sequence identity or complementarity, is between about 60% to about 70%. In preferred embodiments, homology, sequence identity or complementarity, is between about 70% and about 80%. In more preferred embodiments, homology, sequence identity or complementarity, is between about 80% and about 90%. In some preferred embodiments, homology, sequence identity or complementarity, is about 90%, about 92%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99% or about 100%.

According to the present invention, compounds include antisense oligomeric compounds, antisense oligonucleotides, ribozymes, external guide sequence (EGS) oligonucleotides, alternate splicers, primers, probes, and other oligomeric compounds which hybridize to at least a portion of the target nucleic acid. As such, these compounds may be introduced in the form of single-stranded, double-stranded, circular or hairpin oligomeric compounds and may contain structural elements such as internal or terminal bulges or loops. Once introduced to a system, the compounds of the invention may elicit the action of one or more enzymes or structural proteins to effect modification of the target nucleic acid.

One non-limiting example of such an enzyme is RNAse H, a cellular endonuclease which cleaves the RNA strand of an RNA:DNA duplex. It is known in the art that single-stranded antisense compounds which are "DNA-like" elicit RNAse H. Activation of RNase H, therefore, results in cleavage of the RNA target, thereby greatly enhancing the efficiency of oligonucleotide-mediated inhibition of gene expression. Similar roles have been postulated for other ribonucleases such as those in the RNase III and ribonuclease L family of enzymes.

While a suitable form of antisense compound is a single-stranded antisense oligonucleotide, in many species the introduction of double-stranded structures, such as double-stranded RNA (dsRNA) molecules, has been shown to induce potent and specific antisense-mediated reduction of the function of a gene or its associated gene products. This phenomenon occurs in both plants and animals and is believed to have an evolutionary connection to viral defense and transposon silencing.

The first evidence that dsRNA could lead to gene silencing in animals came in 1995 from work in the nematode, Caenorhabditis elegans (Guo and Kempheus, Cell, 1995, 81, 611-620). Montgomery et al. have shown that the primary interference effects of dsRNA are posttranscriptional (Montgomery et al., Proc. Natl. Acad. Sci. USA, 1998, 95, 15502-15507). The posttranscriptional antisense mechanism defined in Caenorhabditis elegans resulting from exposure to double-stranded RNA (dsRNA) has since been designated RNA interference (RNAi). This term has been generalized to mean antisense-mediated gene silencing involving the introduction of dsRNA leading to the sequence-specific reduction of endogenous targeted mRNA levels (Fire et al., Nature, 1998, 391, 806-811). Recently, it has been shown that it is, in fact, the single-stranded RNA oligomers of antisense polarity of the dsRNAs which are the potent inducers of RNAi (Tijsterman et al., Science, 2002, 295, 694-697).

The antisense compounds of the present invention also include modified compounds in which a different base is present at one or more of the nucleotide positions in the compound. For example, if the first nucleotide is an adenosine, modified compounds may be produced which contain thymidine, guanosine or cytidine at this position. This may be done at any of the positions of the antisense compound.

The antisense compounds of the present invention can be utilized for diagnostics, therapeutics, prophylaxis and as research reagents and kits. Furthermore, antisense oligonucleotides, which are able to inhibit gene expression with exquisite specificity, are often used by those of ordinary skill to elucidate the function of particular genes or to distinguish between functions of various members of a biological pathway. Antisense modulation has, therefore, been harnessed for research use.

For use in kits and diagnostics, the compounds of the present invention, either alone or in combination with other compounds or therapeutics, can be used as tools in differential and/or combinatorial analyses to elucidate expression patterns of a portion or the entire complement of genes expressed within cells and tissues.

As one nonlimiting example, expression patterns within cells or tissues treated with one or more antisense compounds are compared to control cells or tissues not treated with antisense compounds and the patterns produced are analyzed for differential levels of gene expression as they pertain, for example, to disease association, signaling pathway, cellular localization, expression level, size, structure or function of the genes examined. These analyses can be performed on stimulated or unstimulated cells and in the presence or absence of other compounds which affect expression patterns.

Examples of methods of gene expression analysis known in the art include DNA arrays or microarrays (Brazma and Vilo, FEBS Lett., 2000, 480, 17-24; Celis, et al., FEBS Lett., 2000, 480, 2-16), SAGE (serial analysis of gene expression)(Madden, et al., Drug Discov. Today, 2000, 5, 415-425), READS (restriction enzyme amplification of digested cDNAs) (Prashar and Weissman, Methods Enzymol., 1999, 303, 258-72), TOGA (total gene expression analysis) (Sutcliffe, et al., Proc. Natl. Acad. Sci. U.S.A., 2000, 97, 1976-81), protein arrays and proteomics (Celis, et al., FEBS Lett., 2000, 480, 2-16; Jungblut, et al., Electrophoresis, 1999, 20, 2100-10), expressed sequence tag (EST) sequencing (Celis, et al., FEBS Lett., 2000, 480, 2-16; Larsson, et al., J. Biotechnol., 2000, 80, 143-57), subtractive RNA fingerprinting (SuRF) (Fuchs, et al., Anal. Biochem., 2000, 286, 91-98; Larson, et al., Cytometry, 2000, 41, 203-208), subtractive cloning, differential display (DD) (Jurecic and Belmont, Curr. Opin. Microbiol., 2000, 3, 316-21), comparative genomic hybridization (Carulli, et al., J. Cell Biochem. Suppl., 1998, 31, 286-96), FISH (fluorescent in situ hybridization) techniques (Going and Gusterson, Eur. J. Cancer, 1999, 35, 1895-904) and mass spectrometry methods (To, Comb. Chem. High Throughput Screen, 2000, 3, 235-41).

The antisense compounds of the invention are useful for research and diagnostics, because these compounds hybridize to nucleic acids encoding PTP1B. For example, oligonucleotides that are shown to hybridize with such efficiency and under such conditions as disclosed herein as to be effective PTP1B inhibitors are effective primers or probes under conditions favoring gene amplification or detection, respectively. These primers and probes are useful in methods requiring the specific detection of nucleic acid molecules encoding PTP1B and in the amplification of said nucleic acid molecules for detection or for use in further studies of PTP1B.

Hybridization of the antisense oligonucleotides, particularly the primers and probes, of the invention with a nucleic acid encoding PTP1B can be detected by means known in the art. Such means may include conjugation of an enzyme to the oligonucleotide, radiolabelling of the oligonucleotide or any other suitable detection means. Kits using such detection means for detecting the level of PTP1B in a sample may also be prepared.

The specificity and sensitivity of antisense are also harnessed by those of skill in the art for therapeutic uses. Antisense oligonucleotides have been employed as therapeutic moieties in the treatment of disease states in animals and man. Antisense oligonucleotides have been safely and effectively administered to humans and numerous clinical trials are presently underway. It is thus established that oligonucleotides can be useful therapeutic modalities that can be configured to be useful in treatment regimes for treatment of cells, tissues and animals, especially humans.

In the context of this invention, the term "oligonucleotide" refers to an oligomer or polymer of ribonucleic acid (RNA) or deoxyribonucleic acid (DNA) or mimetics thereof. This term includes oligonucleotides composed of naturally-occurring nucleobases, sugars and covalent internucleoside (backbone) linkages as well as oligonucleotides having non-naturally-occurring portions which function similarly. Such modified or substituted oligonucleotides are often preferred over native forms because of desirable properties such as, for example, enhanced cellular uptake, enhanced affinity for nucleic acid target and increased stability in the presence of nucleases.

While antisense oligonucleotides are a preferred form of antisense compound, the present invention comprehends other oligomeric antisense compounds, including but not limited to oligonucleotide mimetics such as are described below. The antisense compounds in accordance with this invention preferably comprise from about 8 to about 50 nucleobases (i.e. from about 8 to about 50 linked nucleosides). One having ordinary skill in the art will appreciate that this embodies compounds of 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50 nucleobases in length.

In another embodiment, the antisense compounds of the invention are 15 to 30 nucleobases in length. One having ordinary skill in the art will appreciate that this embodies compounds of 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 nucleobases in length.

Antisense compounds 8-50 nucleobases in length comprising a stretch of at least eight (8) consecutive nucleobases selected from within the illustrative antisense compounds are considered to be suitable antisense compounds as well. Exemplary preferred antisense compounds include oligonucleotide sequences that comprise at least the 8 consecutive nucleobases from the 5'-terminus of one of the illustrative preferred antisense compounds (the remaining nucleobases being a consecutive stretch of the same oligonucleotide beginning immediately upstream of the 5'-terminus of the antisense compound which is specifically hybridizable to the target nucleic acid and continuing until the oligonucleotide contains about 8 to about 50 nucleobases). Similarly preferred antisense compounds are represented by oligonucleotide sequences that comprise at least the 8 consecutive nucleobases from the 3'-terminus of one of the illustrative preferred antisense compounds (the remaining nucleobases being a consecutive stretch of the same oligonucleotide beginning immediately downstream of the 3'-terminus of the antisense compound which is specifically hybridizable to the target nucleic acid and continuing until the oligonucleotide contains about 8 to about 50 nucleobases). It is also understood that preferred antisense compounds may be represented by oligonucleotide sequences that comprise at least 8 consecutive nucleobases from an internal portion of the sequence of an illustrative preferred antisense compound, and may extend in either or both directions until the oligonucleotide contains about 8 to about 50 nucleobases. One having skill in the art armed with the preferred antisense compounds illustrated herein will be able, without undue experimentation, to identify further preferred antisense compounds.

As is known in the art, a nucleoside is a base-sugar combination. The base portion of the nucleoside is normally a heterocyclic base. The two most common classes of such heterocyclic bases are the purines and the pyrimidines. Nucleotides are nucleosides that further include a phosphate group covalently linked to the sugar portion of the nucleoside. For those nucleosides that include a pentofuranosyl sugar, the phosphate group can be linked to either the 2', 3' or 5' hydroxyl moiety of the sugar. In forming oligonucleotides, the phosphate groups covalently link adjacent nucleosides to one another to form a linear polymeric compound. In turn the respective ends of this linear polymeric structure can be further joined to form a circular structure, however, open linear structures are generally preferred. Within the oligonucleotide structure, the phosphate groups are commonly referred to as forming the internucleoside backbone of the oligonucleotide. The normal linkage or backbone of RNA and DNA is a 3' to 5' phosphodiester linkage.

Specific examples of preferred antisense compounds useful in this invention include oligonucleotides containing modified backbones or non-natural internucleoside linkages. As defined in this specification, oligonucleotides having modified backbones include those that retain a phosphorus atom in the backbone and those that do not have a phosphorus atom in the backbone. For the purposes of this specification, and as sometimes referenced in the art, modified oligonucleotides that do not have a phosphorus atom in their internucleoside backbone can also be considered to be oligonucleosides.

Preferred modified oligonucleotide backbones include, for example, phosphorothioates, chiral phosphorothioates, phosphorodithioates, phosphotriesters, aminoalkylphosphotriesters, methyl and other alkyl phosphonates including 3'-alkylene phosphonates and chiral phosphonates, phosphinates, phosphoramidates including 3'-amino phosphoramidate and aminoalkylphosphoramidates, thionophosphoramidates, thionoalkylphosphonates, thionoalkylphosphotriesters, and boranophosphates having normal 3'-5' linkages, 2'-5' linked analogs of these, and those having inverted polarity wherein the adjacent pairs of nucleoside units are linked 3'-5' to 5'-3' or 2'-5' to 5'-2'. Various salts, mixed salts and free acid forms are also included.

Representative United States patents that teach the preparation of the above phosphorus-containing linkages include, but are not limited to, U.S. Pat. Nos. 3,687,808; 4,469,863; 4,476,301; 5,023,243; 5,177,196; 5,188,897; 5,264,423; 5,276,019; 5,278,302; 5,286,717; 5,321,131; 5,399,676; 5,405,939; 5,453,496; 5,455,233; 5,466,677; 5,476,925; 5,519,126; 5,536,821; 5,541,306; 5,550,111; 5,563,253; 5,571,799; 5,587,361; and 5,625,050, certain of which are commonly owned with this application, and each of which is herein incorporated by reference.

Preferred modified oligonucleotide backbones that do not include a phosphorus atom therein have backbones that are formed by short chain alkyl or cycloalkyl internucleoside linkages, mixed heteroatom and alkyl or cycloalkyl internucleoside linkages, or one or more short chain heteroatomic or heterocyclic internucleoside linkages. These include those having morpholino linkages (formed in part from the sugar portion of a nucleoside); siloxane backbones; sulfide, sulfoxide and sulfone backbones; formacetyl and thioformacetyl backbones; methylene formacetyl and thioformacetyl backbones; alkene containing backbones; sulfamate backbones; methyleneimino and methylenehydrazino backbones; sulfonate and sulfonamide backbones; amide backbones; and others having mixed N, O, S and CH.sub.2 component parts.

Representative United States patents that teach the preparation of the above oligonucleosides include, but are not limited to, U.S. Pat. Nos. 5,034,506; 5,166,315; 5,185,444; 5,214,134; 5,216,141; 5,235,033; 5,264,562; 5,264,564; 5,405,938; 5,434,257; 5,466,677; 5,470,967; 5,489,677; 5,541,307; 5,561,225; 5,596,086; 5,602,240; 5,610,289; 5,602,240; 5,608,046; 5,610,289; 5,618,704; 5,623,070; 5,663,312; 5,633,360; 5,677,437; and 5,677,439, certain of which are commonly owned with this application, and each of which is herein incorporated by reference.

In other preferred oligonucleotide mimetics, both the sugar and the internucleoside linkage, i.e., the backbone, of the nucleotide units are replaced with novel groups. The base units are maintained for hybridization with an appropriate nucleic acid target compound. One such oligomeric compound, an oligonucleotide mimetic that has been shown to have excellent hybridization properties, is referred to as a peptide nucleic acid (PNA). In PNA compounds, the sugar-backbone of an oligonucleotide is replaced with an amide containing backbone, in particular an aminoethylglycine backbone. The nucleobases are retained and are bound directly or indirectly to aza nitrogen atoms of the amide portion of the backbone. Representative United States patents that teach the preparation of PNA compounds include, but are not limited to, U.S. Pat. Nos. 5,539,082; 5,714,331; and 5,719,262, each of which is herein incorporated by reference. Further teaching of PNA compounds can be found in Nielsen et al., Science, 1991, 254, 1497-1500.

Most preferred embodiments of the invention are oligonucleotides with phosphorothioate backbones and oligonucleosides with heteroatom backbones, and in particular --CH.sub.2--NH--O--CH.sub.2--, --CH.sub.2--N(CH.sub.3)--O--CH.sub.2-- ((known as a methylene (methylimino) or MMI backbone)), --CH.sub.2--O--N(CH.sub.3)--CH.sub.2--, --CH.sub.2--N(CH.sub.3)--N(CH.sub.3)--CH.sub.2-- and --O--N(CH.sub.3)--CH.sub.2--CH.sub.2-- (wherein the native phosphodiester backbone is represented as --O--P--O--CH.sub.2--) of the above referenced U.S. Pat. No. 5,489,677, and the amide backbones of the above referenced U.S. Pat. No. 5,602,240. Also preferred are oligonucleotides having morpholino backbone structures of the above-referenced U.S. Pat. No. 5,034,506.

Modified oligonucleotides may also contain one or more substituted sugar moieties. Preferred oligonucleotides comprise one of the following at the 2' position: OH; F; O-, S-, or N-alkyl; O-, S-, or N-alkenyl; O-, S- or N-alkynyl; or O-alkyl-O-alkyl, wherein the alkyl, alkenyl and alkynyl may be substituted or unsubstituted C.sub.1 to C.sub.10 alkyl or C.sub.2 to C.sub.10 alkenyl and alkynyl. Particularly preferred are O[(CH.sub.2).sub.nO].sub.mCH.sub.3, O(CH.sub.2).sub.nOCH.sub.3, O(CH.sub.2).sub.nNH.sub.2, O(CH.sub.2).sub.nCH.sub.3, O(CH.sub.2).sub.nONH.sub.2, and O(CH.sub.2).sub.nON[(CH.sub.2).sub.nCH.sub.3)].sub.2, where n and m are from 1 to about 10. Other preferred oligonucleotides comprise one of the following at the 2' position: C.sub.1 to C.sub.10 lower alkyl, substituted lower alkyl, alkaryl, aralkyl, O-alkaryl or O-aralkyl, SH, SCH.sub.3, OCN, Cl, Br, CN, CF.sub.3, OCF.sub.3, SOCH.sub.3, SO.sub.2CH.sub.3, ONO.sub.2, NO.sub.2, N.sub.3, NH.sub.2, heterocycloalkyl, heterocycloalkaryl, aminoalkylamino, polyalkylamino, substituted silyl, an RNA cleaving group, a reporter group, an intercalator, a group for improving the pharmacokinetic properties of an oligonucleotide, or a group for improving the pharmacodynamic properties of an oligonucleotide, and other substituents having similar properties. A preferred modification includes 2'-methoxyethoxy (2'-O--CH.sub.2CH.sub.2OCH.sub.3, also known as 2'-O-(2-methoxyethyl) or 2'-MOE) (Martin et al., Helv. Chim. Acta, 1995, 78, 486-504) i.e., an alkoxyalkoxy group.

A further preferred modification includes 2'-dimethylaminooxyethoxy, i.e., a O(CH.sub.2).sub.2ON(CH.sub.3).sub.2 group, also known as 2'-DMAOE, as described in examples hereinbelow, and 2'-dimethylaminoethoxyethoxy (also known in the art as 2'-O-dimethylaminoethoxyethyl or 2'-DMAEOE), i.e., 2'-O--CH.sub.2--O--CH.sub.2--N(CH.sub.2).sub.2, also described in examples hereinbelow.

Other preferred modifications include 2'-methoxy (2'-O--CH.sub.3), 2'-aminopropoxy (2'-OCH.sub.2CH.sub.2CH.sub.2NH.sub.2) and 2'-fluoro (2'-F). Similar modifications may also be made at other positions on the oligonucleotide, particularly the 3' position of the sugar on the 3' terminal nucleotide or in 2'-5' linked oligonucleotides and the 5' position of 5' terminal nucleotide. Oligonucleotides may also have sugar mimetics such as cyclobutyl moieties in place of the pentofuranosyl sugar. Representative United States patents that teach the preparation of such modified sugar structures include, but are not limited to, U.S. Pat. Nos. 4,981,957; 5,118,800; 5,319,080; 5,359,044; 5,393,878; 5,446,137; 5,466,786; 5,514,785; 5,519,134; 5,567,811; 5,576,427; 5,591,722; 5,597,909; 5,610,300; 5,627,053; 5,639,873; 5,646,265; 5,658,873; 5,670,633; and 5,700,920, certain of which are commonly owned with the instant application, and each of which is herein incorporated by reference in its entirety.

Oligonucleotides may also include nucleobase (often referred to in the art simply as "base") modifications or substitutions. As used herein, "unmodified" or "natural" nucleobases include the purine bases adenine (A) and guanine (G), and the pyrimidine bases thymine (T), cytosine (C) and uracil (U). Modified nucleobases include other synthetic and natural nucleobases such as 5-methylcytosine (5-me-C), 5-hydroxymethyl cytosine, xanthine, hypoxanthine, 2-aminoadenine, 6-methyl and other alkyl derivatives of adenine and guanine, 2-propyl and other alkyl derivatives of adenine and guanine, 2-thiouracil, 2-thiothymine and 2-thiocytosine, 5-halouracil and cytosine, 5-propynyl uracil and cytosine, 6-azo uracil, cytosine and thymine, 5-uracil (pseudouracil), 4-thiouracil, 8-halo, 8-amino, 8-thiol, 8-thioalkyl, 8-hydroxyl and other 8-substituted adenines and guanines, 5-halo particularly 5-bromo, 5-trifluoromethyl and other 5-substituted uracils and cytosines, 7-methylguanine and 7-methyladenine, 8-azaguanine and 8-azaadenine, 7-deazaguanine and 7-deazaadenine and 3-deazaguanine and 3-deazaadenine. Further nucleobases include those disclosed in U.S. Pat. No. 3,687,808, those disclosed in The Concise Encyclopedia Of Polymer Science And Engineering, pages 858-859, Kroschwitz, J. I., ed. John Wiley & Sons, 1990, those disclosed by Englisch et al., Angewandte Chemie, International Edition, 1991, 30, 613, and those disclosed by Sanghvi, Y. S., Chapter 15, Antisense Research and Applications, pages 289-302, Crooke, S. T. and Lebleu, B., ed., CRC Press, 1993. Certain of these nucleobases are particularly useful for increasing the binding affinity of the oligomeric compounds of the invention. These include 5-substituted pyrimidines, 6-azapyrimidines and N-2, N-6 and O-6 substituted purines, including 2-aminopropyladenine, 5-propynyluracil and 5-propynylcytosine. 5-methylcytosine substitutions have been shown to increase nucleic acid duplex stability by 0.6-1.2 C (Sanghvi, Y. S., Crooke, S. T. and Lebleu, B., eds., Antisense Research and Applications, CRC Press, Boca Raton, 1993, pp. 276-278) and are presently preferred base substitutions, even more particularly when combined with 2'-O-methoxyethyl sugar modifications.

Representative United States patents that teach the preparation of certain of the above noted modified nucleobases as well as other modified nucleobases include, but are not limited to, the above noted U.S. Pat. No. 3,687,808, as well as U.S. Pat. Nos. 4,845,205; 5,130,302; 5,134,066; 5,175,273; 5,367,066; 5,432,272; 5,457,187; 5,459,255; 5,484,908; 5,502,177; 5,525,711; 5,552,540; 5,587,469; 5,594,121, 5,596,091; 5,614,617; and 5,681,941, certain of which are commonly owned with the instant application, and each of which is herein incorporated by reference, and U.S. Pat. No. 5,750,692, which is commonly owned with the instant application and also herein incorporated by reference.

Another modification of the oligonucleotides of the invention involves chemically linking to the oligonucleotide one or more moieties or conjugates which enhance the activity, cellular distribution or cellular uptake of the oligonucleotide. Such moieties include but are not limited to lipid moieties such as a cholesterol moiety (Letsinger et al., Proc. Natl. Acad. Sci. USA, 1989, 86, 6553-6556), cholic acid (Manoharan et al., Bioorg. Med. Chem. Let., 1994, 4, 1053-1060), a thioether, e.g., hexyl-5-tritylthiol (Manoharan et al., Ann. N.Y. Acad. Sci., 1992, 660, 306-309; Manoharan et al., Bioorg. Med. Chem. Let., 1993, 3, 2765-2770), a thiocholesterol (Oberhauser et al., Nucl. Acids Res., 1992, 20, 533-538), an aliphatic chain, e.g., dodecandiol or undecyl residues (Saison-Behmoaras et al., EMBO J., 1991, 10, 1111-1118; Kabanov et al., FEBS Lett., 1990, 259, 327-330; Svinarchuk et al., Biochimie, 1993, 75, 49-54), a phospholipid, e.g., di-hexadecyl-rac-glycerol or triethylammonium 1,2-di-O-hexadecyl-rac-glycero-3-H-phosphonate (Manoharan et al., Tetrahedron Lett., 1995, 36, 3651-3654; Shea et al., Nucl. Acids Res., 1990, 18, 3777-3783), a polyamine or a polyethylene glycol chain (Manoharan et al., Nucleosides & Nucleotides, 1995, 14, 969-973), or adamantane acetic acid (Manoharan et al., Tetrahedron Lett., 1995, 36, 3651-3654), a palmityl moiety (Mishra et al., Biochim. Biophys. Acta, 1995, 1264, 229-237), or an octadecylamine or hexylamino-carbonyl-oxycholesterol moiety (Crooke et al., J. Pharmacol. Exp. Ther., 1996, 277, 923-937.

Representative United States patents that teach the preparation of such oligonucleotide conjugates include, but are not limited to, U.S. Pat. Nos. 4,828,979; 4,948,882; 5,218,105; 5,525,465; 5,541,313; 5,545,730; 5,552,538; 5,578,717, 5,580,731; 5,580,731; 5,591,584; 5,109,124; 5,118,802; 5,138,045; 5,414,077; 5,486,603; 5,512,439; 5,578,718; 5,608,046; 4,587,044; 4,605,735; 4,667,025; 4,762,779; 4,789,737; 4,824,941; 4,835,263; 4,876,335; 4,904,582; 4,958,013; 5,082,830; 5,112,963; 5,214,136; 5,082,830; 5,112,963; 5,214,136; 5,245,022; 5,254,469; 5,258,506; 5,262,536; 5,272,250; 5,292,873; 5,317,098; 5,371,241, 5,391,723; 5,416,203, 5,451,463; 5,510,475; 5,512,667; 5,514,785; 5,565,552; 5,567,810; 5,574,142; 5,585,481; 5,587,371; 5,595,726; 5,597,696; 5,599,923; 5,599,928 and 5,688,941, certain of which are commonly owned with the instant application, and each of which is herein incorporated by reference.

It is not necessary for all positions in a given compound to be uniformly modified, and in fact more than one of the aforementioned modifications may be incorporated in a single compound or even at a single nucleoside within an oligonucleotide. The present invention also includes antisense compounds which are chimeric compounds. "Chimeric" antisense compounds or "chimeras," in the context of this invention, are antisense compounds, particularly oligonucleotides, which contain two or more chemically distinct regions, each made up of at least one monomer unit, i.e., a nucleotide in the case of an oligonucleotide compound. These oligonucleotides typically contain at least one region wherein the oligonucleotide is modified so as to confer upon the oligonucleotide increased resistance to nuclease degradation, increased cellular uptake, and/or increased binding affinity for the target nucleic acid. An additional region of the oligonucleotide may serve as a substrate for enzymes capable of cleaving RNA:DNA or RNA:RNA hybrids. By way of example, RNase H is a cellular endonuclease which cleaves the RNA strand of an RNA:DNA duplex. Activation of RNase H, therefore, results in cleavage of the RNA target, thereby greatly enhancing the efficiency of oligonucleotide inhibition of gene expression. Consequently, comparable results can often be obtained with shorter oligonucleotides when chimeric oligonucleotides are used, compared to phosphorothioate deoxyoligonucleotides hybridizing to the same target region. Cleavage of the RNA target can be routinely detected by gel electrophoresis and, if necessary, associated nucleic acid hybridization techniques known in the art.

Chimeric antisense compounds of the invention may be formed as composite structures of two or more oligonucleotides, modified oligonucleotides, oligonucleosides and/or oligonucleotide mimetics as described above. Such compounds have also been referred to in the art as hybrids or gapmers. Representative United States patents that teach the preparation of such hybrid structures include, but are not limited to, U.S. Pat. Nos. 5,013,830; 5,149,797; 5,220,007; 5,256,775; 5,366,878; 5,403,711; 5,491,133; 5,565,350; 5,623,065; 5,652,355; 5,652,356; and 5,700,922, certain of which are commonly owned with the instant application, and each of which is herein incorporated by reference in its entirety.

The antisense compounds used in accordance with this invention may be conveniently and routinely made through the well-known technique of solid phase synthesis. Equipment for such synthesis is sold by several vendors including, for example, Applied Biosystems (Foster City, Calif.). Any other means for such synthesis known in the art may additionally or alternatively be employed. It is well known to use similar techniques to prepare oligonucleotides such as the phosphorothioates and alkylated derivatives.

The antisense compounds of the invention are synthesized in vitro and do not include antisense compositions of biological origin, or genetic vector constructs designed to direct the in vivo synthesis of antisense molecules.

The compounds of the invention may also be admixed, encapsulated, conjugated or otherwise associated with other molecules, molecule structures or mixtures of compounds, as for example, liposomes, receptor targeted molecules, oral, rectal, topical or other formulations, for assisting in uptake, distribution and/or absorption. Representative United States patents that teach the preparation of such uptake, distribution and/or absorption assisting formulations include, but are not limited to, U.S. Pat. Nos. 5,108,921; 5,354,844; 5,416,016; 5,459,127; 5,521,291; 5,543,158; 5,547,932; 5,583,020; 5,591,721; 4,426,330; 4,534,899; 5,013,556; 5,108,921; 5,213,804; 5,227,170; 5,264,221; 5,356,633; 5,395,619; 5,416,016; 5,417,978; 5,462,854; 5,469,854; 5,512,295; 5,527,528; 5,534,259; 5,543,152; 5,556,948; 5,580,575; and 5,595,756, each of which is herein incorporated by reference.

The antisense compounds of the invention encompass any pharmaceutically acceptable salts, esters, or salts of such esters, or any other compound which, upon administration to an animal including a human, is capable of providing (directly or indirectly) the biologically active metabolite or residue thereof. Accordingly, for example, the disclosure is also drawn to prodrugs and pharmaceutically acceptable salts of the compounds of the invention, pharmaceutically acceptable salts of such prodrugs, and other bioequivalents.

The term "prodrug" indicates a therapeutic agent that is prepared in an inactive form that is converted to an active form (i.e., drug) within the body or cells thereof by the action of endogenous enzymes or other chemicals and/or conditions. In particular, prodrug versions of the oligonucleotides of the invention are prepared as SATE [(S-acetyl-2-thioethyl) phosphate] derivatives according to the methods disclosed in WO 93/24510 to Gosselin et al., published Dec. 9, 1993 or in WO 94/26764 to Imbach et al.

The term "pharmaceutically acceptable salts" refers to physiologically and pharmaceutically acceptable salts of the compounds of the invention: i.e., salts that retain the desired biological activity of the parent compound and do not impart undesired toxicological effects thereto.

Pharmaceutically acceptable base addition salts are formed with metals or amines, such as alkali and alkaline earth metals or organic amines. Examples of metals used as cations are sodium, potassium, magnesium, calcium, and the like. Examples of suitable amines are N,N'-dibenzylethylenediamine, chloroprocaine, choline, diethanolamine, dicyclohexylamine, ethylenediamine, N-methylglucamine, and procaine (see, for example, Berge et al., "Pharmaceutical Salts," J. of Pharma Sci., 1977, 66, 1-19). The base addition salts of said acidic compounds are prepared by contacting the free acid form with a sufficient amount of the desired base to produce the salt in the conventional manner. The free acid form may be regenerated by contacting the salt form with an acid, and isolating the free acid in the conventional manner. The free acid forms differ from their respective salt forms somewhat in certain physical properties such as solubility in polar solvents, but otherwise the salts are equivalent to their respective free acid for purposes of the present invention. As used herein, a "pharmaceutical addition salt" includes a pharmaceutically acceptable salt of an acid form of one of the components of the compositions of the invention. These include organic or inorganic acid salts of the amines. Preferred acid salts are the hydrochlorides, acetates, salicylates, nitrates and phosphates. Other suitable pharmaceutically acceptable salts are well known to those skilled in the art and include basic salts of a variety of inorganic and organic acids, such as, for example, with inorganic acids, such as for example hydrochloric acid, hydrobromic acid, sulfuric acid or phosphoric acid; with organic carboxylic, sulfonic, sulfo or phospho acids or N-substituted sulfamic acids, for example acetic acid, propionic acid, glycolic acid, succinic acid, maleic acid, hydroxymaleic acid, methylmaleic acid, fumaric acid, malic acid, tartaric acid, lactic acid, oxalic acid, gluconic acid, glucaric acid, glucuronic acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, salicylic acid, 4-aminosalicylic acid, 2-phenoxybenzoic acid, 2-acetoxybenzoic acid, embonic acid, nicotinic acid or isonicotinic acid; and with amino acids, such as the 20 alpha-amino acids involved in the synthesis of proteins in nature, for example glutamic acid or aspartic acid, and also with phenylacetic acid, methanesulfonic acid, ethanesulfonic acid, 2-hydroxyethanesulfonic acid, ethane-1,2-disulfonic acid, benzenesulfonic acid, 4-methylbenzenesulfoc acid, naphthalene-2-sulfonic acid, naphthalene-1,5-disulfonic acid, 2- or 3-phosphoglycerate, glucose-6-phosphate, N-cyclohexylsulfamic acid (with the formation of cyclamates), or with other acid organic compounds, such as ascorbic acid. Pharmaceutically acceptable salts of compounds may also be prepared with a pharmaceutically acceptable cation. Suitable pharmaceutically acceptable cations are well known to those skilled in the art and include alkaline, alkaline earth, ammonium and quaternary ammonium cations. Carbonates or hydrogen carbonates are also possible.

For oligonucleotides, preferred examples of pharmaceutically acceptable salts include but are not limited to (a) salts formed with cations such as sodium, potassium, ammonium, magnesium, calcium, polyamines such as spermine and spermidine, etc.; (b) acid addition salts formed with inorganic acids, for example hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, nitric acid and the like; (c) salts formed with organic acids such as, for example, acetic acid, oxalic acid, tartaric acid, succinic acid, maleic acid, fumaric acid, gluconic acid, citric acid, malic acid, ascorbic acid, benzoic acid, tannic acid, palmitic acid, alginic acid, polyglutamic acid, naphthalenesulfonic acid, methanesulfonic acid, p-toluenesulfonic acid, naphthalenedisulfonic acid, polygalacturonic acid, and the like; and (d) salts formed from elemental anions such as chlorine, bromine, and iodine.

The antisense compounds of the present invention can be utilized for diagnostics, therapeutics, prophylaxis and as research reagents and kits. For therapeutics, an animal, preferably a human, suspected of having a disease or disorder, which can be treated by modulating the expression of PTP1B, is treated by administering antisense compounds in accordance with this invention. The compounds of the invention can be utilized in pharmaceutical compositions by adding an effective amount of an antisense compound to a suitable pharmaceutically acceptable diluent or carrier. Use of the antisense compounds and methods of the invention may also be useful prophylactically, e.g., to prevent or delay infection, inflammation or tumor formation, for example.

The antisense compounds of the invention are useful for research and diagnostics, because these compounds hybridize to nucleic acids encoding PTP1B, enabling sandwich and other assays to easily be constructed to exploit this fact. Hybridization of the antisense oligonucleotides of the invention with a nucleic acid encoding PTP1B can be detected by means known in the art. Such means may include conjugation of an enzyme to the oligonucleotide, radiolabelling of the oligonucleotide or any other suitable detection means. Kits using such detection means for detecting the level of PTP1B in a sample may also be prepared.

The present invention also includes pharmaceutical compositions and formulations which include the antisense compounds of the invention. The pharmaceutical compositions of the present invention may be administered in a number of ways depending upon whether local or systemic treatment is desired and upon the area to be treated. Administration may be topical (including ophthalmic and to mucous membranes including vaginal and rectal delivery), pulmonary, e.g., by inhalation or insufflation of powders or aerosols, including by nebulizer; intratracheal, intranasal, epidermal and transdermal), oral or parenteral. Parenteral administration includes intravenous, intraarterial, subcutaneous, intraperitoneal or intramuscular injection or infusion; or intracranial, e.g., intrathecal or intraventricular, administration. Oligonucleotides with at least one 2'-O-methoxyethyl modification are believed to be particularly useful for oral administration.

Pharmaceutical compositions and formulations for topical administration may include transdermal patches, ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders. Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable. Coated condoms, gloves and the like may also be useful.

Compositions and formulations for oral administration include powders or granules, suspensions or solutions in water or non-aqueous media, capsules, sachets or tablets. Thickeners, flavoring agents, diluents, emulsifiers, dispersing aids or binders may be desirable.

Compositions and formulations for parenteral, intrathecal or intraventricular administration may include sterile aqueous solutions which may also contain buffers, diluents and other suitable additives such as, but not limited to, penetration enhancers, carrier compounds and other pharmaceutically acceptable carriers or excipients.

Pharmaceutical compositions of the present invention include, but are not limited to, solutions, emulsions, and liposome-containing formulations. These compositions may be generated from a variety of components that include, but are not limited to, preformed liquids, self-emulsifying solids and self-emulsifying semisolids.

The pharmaceutical formulations of the present invention, which may conveniently be presented in unit dosage form, may be prepared according to conventional techniques well known in the pharmaceutical industry. Such techniques include the step of bringing into association the active ingredients with the pharmaceutical carrier(s) or excipient(s). In general the formulations are prepared by uniformly and intimately bringing into association the active ingredients with liquid carriers or finely divided solid carriers or both, and then, if necessary, shaping the product.

The compositions of the present invention may be formulated into any of many possible dosage forms such as, but not limited to, tablets, capsules, liquid syrups, soft gels, suppositories, and enemas. The compositions of the present invention may also be formulated as suspensions in aqueous, non-aqueous or mixed media. Aqueous suspensions may further contain substances which increase the viscosity of the suspension including, for example, sodium carboxymethylcellulose, sorbitol and/or dextran. The suspension may also contain stabilizers.

In one embodiment of the present invention the pharmaceutical compositions may be formulated and used as foams. Pharmaceutical foams include formulations such as, but not limited to, emulsions, microemulsions, creams, jellies and liposomes. While basically similar in nature these formulations vary in the components and the consistency of the final product. The preparation of such compositions and formulations is generally known to those skilled in the pharmaceutical and formulation arts and may be applied to the formulation of the compositions of the present invention.

Emulsions

The compositions of the present invention may be prepared and formulated as emulsions. Emulsions are typically heterogenous systems of one liquid dispersed in another in the form of droplets usually exceeding 0.1 m in diameter. (Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199; Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., Volume 1, p. 245; Block in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 2, p. 335; Higuchi et al., in Remington's Pharmaceutical Sciences, Mack Publishing Co., Easton, Pa., 1985, p. 301). Emulsions are often biphasic systems comprising of two immiscible liquid phases intimately mixed and dispersed with each other. In general, emulsions may be either water-in-oil (w/o) or of the oil-in-water (o/w) variety. When an aqueous phase is finely divided into and dispersed as minute droplets into a bulk oily phase the resulting composition is called a water-in-oil (w/o) emulsion. Alternatively, when an oily phase is finely divided into and dispersed as minute droplets into a bulk aqueous phase the resulting composition is called an oil-in-water (o/w) emulsion. Emulsions may contain additional components in addition to the dispersed phases and the active drug which may be present as a solution in either the aqueous phase, oily phase or itself as a separate phase. Pharmaceutical excipients such as emulsifiers, stabilizers, dyes, and anti-oxidants may also be present in emulsions as needed. Pharmaceutical emulsions may also be multiple emulsions that are comprised of more than two phases such as, for example, in the case of oil-in-water-in-oil (o/w/o) and water-in-oil-in-water (w/o/w) emulsions. Such complex formulations often provide certain advantages that simple binary emulsions do not. Multiple emulsions in which individual oil droplets of an o/w emulsion enclose small water droplets constitute a w/o/w emulsion. Likewise a system of oil droplets enclosed in globules of water stabilized in an oily continuous provides an o/w/o emulsion.

Emulsions are characterized by little or no thermodynamic stability. Often, the dispersed or discontinuous phase of the emulsion is well dispersed into the external or continuous phase and maintained in this form through the means of emulsifiers or the viscosity of the formulation. Either of the phases of the emulsion may be a semisolid or a solid, as is the case of emulsion-style ointment bases and creams. Other means of stabilizing emulsions entail the use of emulsifiers that may be incorporated into either phase of the emulsion. Emulsifiers may broadly be classified into four categories: synthetic surfactants, naturally occurring emulsifiers, absorption bases, and finely dispersed solids (Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199).

Synthetic surfactants, also known as surface active agents, have found wide applicability in the formulation of emulsions and have been reviewed in the literature (Rieger, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 285; Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), Marcel Dekker, Inc., New York, N.Y., 1988, volume 1, p. 199). Surfactants are typically amphiphilic and comprise a hydrophilic and a hydrophobic portion. The ratio of the hydrophilic to the hydrophobic nature of the surfactant has been termed the hydrophile/lipophile balance (HLB) and is a valuable tool in categorizing and selecting surfactants in the preparation of formulations. Surfactants may be classified into different classes based on the nature of the hydrophilic group: nonionic, anionic, cationic and amphoteric (Rieger, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 285).

Naturally occurring emulsifiers used in emulsion formulations include lanolin, beeswax, phosphatides, lecithin and acacia. Absorption bases possess hydrophilic properties such that they can soak up water to form w/o emulsions yet retain their semisolid consistencies, such as anhydrous lanolin and hydrophilic petrolatum. Finely divided solids have also been used as good emulsifiers especially in combination with surfactants and in viscous preparations. These include polar inorganic solids, such as heavy metal hydroxides, nonswelling clays such as bentonite, attapulgite, hectorite, kaolin, montmorillonite, colloidal aluminum silicate and colloidal magnesium aluminum silicate, pigments and nonpolar solids such as carbon or glyceryl tristearate.

A large variety of non-emulsifying materials are also included in emulsion formulations and contribute to the properties of emulsions. These include fats, oils, waxes, fatty acids, fatty alcohols, fatty esters, humectants, hydrophilic colloids, preservatives and antioxidants (Block, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 335; Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199).

Hydrophilic colloids or hydrocolloids include naturally occurring gums and synthetic polymers such as polysaccharides (for example, acacia, agar, alginic acid, carrageenan, guar gum, karaya gum, and tragacanth), cellulose derivatives (for example, carboxymethylcellulose and carboxypropylcellulose), and synthetic polymers (for example, carbomers, cellulose ethers, and carboxyvinyl polymers). These disperse or swell in water to form colloidal solutions that stabilize emulsions by forming strong interfacial films around the dispersed-phase droplets and by increasing the viscosity of the external phase.

Since emulsions often contain a number of ingredients such as carbohydrates, proteins, sterols and phosphatides that may readily support the growth of microbes, these formulations often incorporate preservatives. Commonly used preservatives included in emulsion formulations include methyl paraben, propyl paraben, quaternary ammonium salts, benzalkonium chloride, esters of p-hydroxybenzoic acid, and boric acid. Antioxidants are also commonly added to emulsion formulations to prevent deterioration of the formulation. Antioxidants used may be free radical scavengers such as tocopherols, alkyl gallates, butylated hydroxyanisole, butylated hydroxytoluene, or reducing agents such as ascorbic acid and sodium metabisulfite, and antioxidant synergists such as citric acid, tartaric acid, and lecithin.

The application of emulsion formulations via dermatological, oral and parenteral routes and methods for their manufacture have been reviewed in the literature (Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199). Emulsion formulations for oral delivery have been very widely used because of reasons of ease of formulation, efficacy from an absorption and bioavailability standpoint. (Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245; Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199). Mineral-oil base laxatives, oil-soluble vitamins and high fat nutritive preparations are among the materials that have commonly been administered orally as o/w emulsions.

In one embodiment of the present invention, the compositions of oligonucleotides and nucleic acids are formulated as microemulsions. A microemulsion may be defined as a system of water, oil and amphiphile which is a single optically isotropic and thermodynamically stable liquid solution (Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245). Typically microemulsions are systems that are prepared by first dispersing an oil in an aqueous surfactant solution and then adding a sufficient amount of a fourth component, generally an intermediate chain-length alcohol to form a transparent system. Therefore, microemulsions have also been described as thermodynamically stable, isotropically clear dispersions of two immiscible liquids that are stabilized by interfacial films of surface-active molecules (Leung and Shah, in: Controlled Release of Drugs: Polymers and Aggregate Systems, Rosoff, M., Ed., 1989, VCH Publishers, New York, pages 185-215). Microemulsions commonly are prepared via a combination of three to five components that include oil, water, surfactant, cosurfactant and electrolyte. Whether the microemulsion is of the water-in-oil (w/o) or an oil-in-water (o/w) type is dependent on the properties of the oil and surfactant used and on the structure and geometric packing of the polar heads and hydrocarbon tails of the surfactant molecules (Schott, in Remington's Pharmaceutical Sciences, Mack Publishing Co., Easton, Pa., 1985, p. 271).

The phenomenological approach utilizing phase diagrams has been extensively studied and has yielded a comprehensive knowledge, to one skilled in the art, of how to formulate microemulsions (Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245; Block, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 335). Compared to conventional emulsions, microemulsions offer the advantage of solubilizing water-insoluble drugs in a formulation of thermodynamically stable droplets that are formed spontaneously.

Surfactants used in the preparation of microemulsions include, but are not limited to, ionic surfactants, non-ionic surfactants, Brij 96, polyoxyethylene oleyl ethers, polyglycerol fatty acid esters, tetraglycerol monolaurate (ML310), tetraglycerol monooleate (MO310), hexaglycerol monooleate (PO310), hexaglycerol pentaoleate (PO500), decaglycerol monocaprate (MCA750), decaglycerol monooleate (MO750), decaglycerol sequioleate (SO750), decaglycerol decaoleate (DAO750), alone or in combination with cosurfactants. The cosurfactant, usually a short-chain alcohol such as ethanol, 1-propanol, and 1-butanol, serves to increase the interfacial fluidity by penetrating into the surfactant film and consequently creating a disordered film because of the void space generated among surfactant molecules. Microemulsions may, however, be prepared without the use of cosurfactants and alcohol-free self-emulsifying microemulsion systems are known in the art. The aqueous phase may typically be, but is not limited to, water, an aqueous solution of the drug, glycerol, PEG300, PEG400, polyglycerols, propylene glycols, and derivatives of ethylene glycol. The oil phase may include, but is not limited to, materials such as Captex 300, Captex 355, Capmul MCM, fatty acid esters, medium chain (C8-C12) mono, di, and tri-glycerides, polyoxyethylated glyceryl fatty acid esters, fatty alcohols, polyglycolized glycerides, saturated polyglycolized C8-C10 glycerides, vegetable oils and silicone oil.

Microemulsions are particularly of interest from the standpoint of drug solubilization and the enhanced absorption of drugs. Lipid based microemulsions (both o/w and w/o) have been proposed to enhance the oral bioavailability of drugs, including peptides (Constantinides et al., Pharmaceutical Research, 1994, 11, 1385-1390; Ritschel, Meth. Find. Exp. Clin. Pharmacol., 1993, 13, 205). Microemulsions afford advantages of improved drug solubilization, protection of drug from enzymatic hydrolysis, possible enhancement of drug absorption due to surfactant-induced alterations in membrane fluidity and permeability, ease of preparation, ease of oral administration over solid dosage forms, improved clinical potency, and decreased toxicity (Constantinides et al., Pharmaceutical Research, 1994, 11, 1385; Ho et al., J. Pharm. Sci., 1996, 85, 138-143). Often microemulsions may form spontaneously when their components are brought together at ambient temperature. This may be particularly advantageous when formulating thermolabile drugs, peptides or oligonucleotides. Microemulsions have also been effective in the transdermal delivery of active components in both cosmetic and pharmaceutical applications. It is expected that the microemulsion compositions and formulations of the present invention will facilitate the increased systemic absorption of oligonucleotides and nucleic acids from the gastrointestinal tract, as well as improve the local cellular uptake of oligonucleotides and nucleic acids within the gastrointestinal tract, vagina, buccal cavity and other areas of administration.

Microemulsions of the present invention may also contain additional components and additives such as sorbitan monostearate (Grill 3), Labrasol, and penetration enhancers to improve the properties of the formulation and to enhance the absorption of the oligonucleotides and nucleic acids of the present invention. Penetration enhancers used in the microemulsions of the present invention may be classified as belonging to one of five broad categories--surfactants, fatty acids, bile salts, chelating agents, and non-chelating non-surfactants (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p. 92). Each of these classes has been discussed above.

Liposomes

There are many organized surfactant structures besides microemulsions that have been studied and used for the formulation of drugs. These include monolayers, micelles, bilayers and vesicles. Vesicles, such as liposomes, have attracted great interest because of their specificity and the duration of action they offer from the standpoint of drug delivery. As used in the present invention, the term "liposome" means a vesicle composed of amphiphilic lipids arranged in a spherical bilayer or bilayers.

Liposomes are unilamellar or multilamellar vesicles which have a membrane formed from a lipophilic material and an aqueous interior. The aqueous portion contains the composition to be delivered. Cationic liposomes possess the advantage of being able to fuse to the cell wall. Non-cationic liposomes, although not able to fuse as efficiently with the cell wall, are taken up by macrophages in vivo.

In order to cross intact mammalian skin, lipid vesicles must pass through a series of fine pores, each with a diameter less than 50 nm, under the influence of a suitable transdermal gradient. Therefore, it is desirable to use a liposome which is highly deformable and able to pass through such fine pores.

Further advantages of liposomes include; liposomes obtained from natural phospholipids are biocompatible and biodegradable; liposomes can incorporate a wide range of water and lipid soluble drugs; liposomes can protect encapsulated drugs in their internal compartments from metabolism and degradation (Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245). Important considerations in the preparation of liposome formulations are the lipid surface charge, vesicle size and the aqueous volume of the liposomes.

Liposomes are useful for the transfer and delivery of active ingredients to the site of action. Because the liposomal membrane is structurally similar to biological membranes, when liposomes are applied to a tissue, the liposomes start to merge with the cellular membranes. As the merging of the liposome and cell progresses, the liposomal contents are emptied into the cell where the active agent may act.

Liposomal formulations have been the focus of extensive investigation as the mode of delivery for many drugs. There is growing evidence that for topical administration, liposomes present several advantages over other formulations. Such advantages include reduced side-effects related to high systemic absorption of the administered drug, increased accumulation of the administered drug at the desired target, and the ability to administer a wide variety of drugs, both hydrophilic and hydrophobic, into the skin.

Several reports have detailed the ability of liposomes to deliver agents including high-molecular weight DNA into the skin. Compounds including analgesics, antibodies, hormones and high-molecular weight DNAs have been administered to the skin. The majority of applications resulted in the targeting of the upper epidermis.

Liposomes fall into two broad classes. Cationic liposomes are positively charged liposomes which interact with the negatively charged DNA molecules to form a stable complex. The positively charged DNA/liposome complex binds to the negatively charged cell surface and is internalized in an endosome. Due to the acidic pH within the endosome, the liposomes are ruptured, releasing their contents into the cell cytoplasm (Wang et al., Biochem. Biophys. Res. Commun., 1987, 147, 980-985).

Liposomes which are pH-sensitive or negatively-charged, entrap DNA rather than complex with it. Since both the DNA and the lipid are similarly charged, repulsion rather than complex formation occurs. Nevertheless, some DNA is entrapped within the aqueous interior of these liposomes. pH-sensitive liposomes have been used to deliver DNA encoding the thymidine kinase gene to cell monolayers in culture. Expression of the exogenous gene was detected in the target cells (Zhou et al., Journal of Controlled Release, 1992, 19, 269-274).

One major type of liposomal composition includes phospholipids other than naturally-derived phosphatidyl-choline. Neutral liposome compositions, for example, can be formed from dimyristoyl phosphatidylcholine (DMPC) or dipalmitoyl phosphatidylcholine (DPPC). Anionic liposome compositions generally are formed from dimyristoyl phosphatidylglycerol, while anionic fusogenic liposomes are formed primarily from dioleoyl phosphatidylethanol-amine (DOPE). Another type of liposomal composition is formed from phosphatidylcholine (PC) such as, for example, soybean PC, and egg PC. Another type is formed from mixtures of phospholipid and/or phosphatidylcholine and/or cholesterol.

Several studies have assessed the topical delivery of liposomal drug formulations to the skin. Application of liposomes containing interferon to guinea pig skin resulted in a reduction of skin herpes sores while delivery of interferon via other means (e.g. as a solution or as an emulsion) were ineffective (Weiner et al., Journal of Drug Targeting, 1992, 2, 405-410). Further, an additional study tested the efficacy of interferon administered as part of a liposomal formulation to the administration of interferon using an aqueous system, and concluded that the liposomal formulation was superior to aqueous administration (du Plessis et al., Antiviral Research, 1992, 18, 259-265).

Non-ionic liposomal systems have also been examined to determine their utility in the delivery of drugs to the skin, in particular systems comprising non-ionic surfactant and cholesterol. Non-ionic liposomal formulations comprising Novasome.TM. I (glyceryl dilaurate/cholesterol/polyoxyethylene-10-stearyl ether) and Novasome.TM. II (glyceryl distearate/cholesterol/polyoxyethylene-10-stearyl ether) were used to deliver cyclosporin-A into the dermis of mouse skin. Results indicated that such non-ionic liposomal systems were effective in facilitating the deposition of cyclosporin-A into different layers of the skin (Hu et al. S.T.P.Pharma. Sci., 1994, 4, 6, 466).

Liposomes also include "sterically stabilized" liposomes, a term which, as used herein, refers to liposomes comprising one or more specialized lipids that, when incorporated into liposomes, result in enhanced circulation lifetimes relative to liposomes lacking such specialized lipids. Examples of sterically stabilized liposomes are those in which part of the vesicle-forming lipid portion of the liposome (A) comprises one or more glycolipids, such as monosialoganglioside G.sub.M1, or (B) is derivatized with one or more hydrophilic polymers, such as a polyethylene glycol (PEG) moiety. While not wishing to be bound by any particular theory, it is thought in the art that, at least for sterically stabilized liposomes containing gangliosides, sphingomyelin, or PEG-derivatized lipids, the enhanced circulation half-life of these sterically stabilized liposomes derives from a reduced uptake into cells of the reticuloendothelial system (RES) (Allen et al., FEBS Letters, 1987, 223, 42; Wu et al., Cancer Research, 1993, 53, 3765). Various liposomes comprising one or more glycolipids are known in the art. Papahadjopoulos et al. (Ann. N.Y. Acad. Sci., 1987, 507, 64) reported the ability of monosialoganglioside G.sub.M1, galactocerebroside sulfate and phosphatidylinositol to improve blood half-lives of liposomes. These findings were expounded upon by Gabizon et al. (Proc. Natl. Acad. Sci. U.S.A., 1988, 85, 6949). U.S. Pat. No. 4,837,028 and WO 88/04924, both to Allen et al., disclose liposomes comprising (1) sphingomyelin and (2) the ganglioside G.sub.M1 or a galactocerebroside sulfate ester. U.S. Pat. No. 5,543,152 (Webb et al.) discloses liposomes comprising sphingomyelin. Liposomes comprising 1,2-sn-dimyristoylphosphatidylcholine are disclosed in WO 97/13499 (Lim et al.).

Many liposomes comprising lipids derivatized with one or more hydrophilic polymers, and methods of preparation thereof, are known in the art. Sunamoto et al. (Bull. Chem. Soc. Jpn., 1980, 53, 2778) described liposomes comprising a nonionic detergent, 2C.sub.1215G, that contains a PEG moiety. Ilium et al. (FEBS Lett., 1984, 167, 79) noted that hydrophilic coating of polystyrene particles with polymeric glycols results in significantly enhanced blood half-lives. Synthetic phospholipids modified by the attachment of carboxylic groups of polyalkylene glycols (e.g., PEG) are described by Sears (U.S. Pat. Nos. 4,426,330 and 4,534,899). Klibanov et al. (FEBS Lett., 1990, 268, 235) described experiments demonstrating that liposomes comprising phosphatidyl-ethanolamine (PE) derivatized with PEG or PEG stearate have significant increases in blood circulation half-lives. Blume et al. (Biochimica et Biophysica Acta, 1990, 1029, 91) extended such observations to other PEG-derivatized phospholipids, e.g., DSPE-PEG, formed from the combination of distearoylphosphatidylethanolamine (DSPE) and PEG. Liposomes having covalently bound PEG moieties on their external surface are described in European Patent No. EP 0 445 131B1 and WO 90/04384 to Fisher. Liposome compositions containing 1-20 mole percent of PE derivatized with PEG, and methods of use thereof, are described by Woodle et al. (U.S. Pat. Nos. 5,013,556 and 5,356,633) and Martin et al. (U.S. Pat. No. 5,213,804 and European Patent No. EP 0 496 813 B1). Liposomes comprising a number of other lipid-polymer conjugates are disclosed in WO 91/05545 and U.S. Pat. No. 5,225,212 (both to Martin et al.) and in WO 94/20073 (Zalipsky et al.) Liposomes comprising PEG-modified ceramide lipids are described in WO 96/10391 (Choi et al.). U.S. Pat. No. 5,540,935 (Miyazaki et al.) and U.S. Pat. No. 5,556,948 (Tagawa et al.) describe PEG-containing liposomes that can be further derivatized with functional moieties on their surfaces.

A limited number of liposomes comprising nucleic acids are known in the art. WO 96/40062 to Thierry et al. discloses methods for encapsulating high molecular weight nucleic acids in liposomes. U.S. Pat. No. 5,264,221 to Tagawa et al. discloses protein-bonded liposomes and asserts that the contents of such liposomes may include an antisense RNA. U.S. Pat. No. 5,665,710 to Rahman et al. describes certain methods of encapsulating oligodeoxy-nucleotides in liposomes. WO 97/04787 to Love et al. discloses liposomes comprising antisense oligonucleotides targeted to the raf gene.

Transfersomes are yet another type of liposomes, and are highly deformable lipid aggregates which are attractive candidates for drug delivery vehicles. Transfersomes may be described as lipid droplets which are so highly deformable that they are easily able to penetrate through pores which are smaller than the droplet. Transfersomes are adaptable to the environment in which they are used, e.g. they are self-optimizing (adaptive to the shape of pores in the skin), self-repairing, frequently reach their targets without fragmenting, and often self-loading. To make transfersomes it is possible to add surface edge-activators, usually surfactants, to a standard liposomal composition. Transfersomes have been used to deliver serum albumin to the skin. The transfersome-mediated delivery of serum albumin has been shown to be as effective as subcutaneous injection of a solution containing serum albumin.

Surfactants find wide application in formulations such as emulsions (including microemulsions) and liposomes. The most common way of classifying and ranking the properties of the many different types of surfactants, both natural and synthetic, is by the use of the hydrophile/lipophile balance (HLB). The nature of the hydrophilic group (also known as the "head") provides the most useful means for categorizing the different surfactants used in formulations (Rieger, in Pharmaceutical Dosage Forms, Marcel Dekker, Inc., New York, N.Y., 1988, p. 285).

If the surfactant molecule is not ionized, it is classified as a nonionic surfactant. Nonionic surfactants find wide application in pharmaceutical and cosmetic products and are usable over a wide range of pH values. In general their HLB values range from 2 to about 18 depending on their structure. Nonionic surfactants include nonionic esters such as ethylene glycol esters, propylene glycol esters, glyceryl esters, polyglyceryl esters, sorbitan esters, sucrose esters, and ethoxylated esters. Nonionic alkanolamides and ethers such as fatty alcohol ethoxylates, propoxylated alcohols, and ethoxylated/propoxylated block polymers are also included in this class. The polyoxyethylene surfactants are the most popular members of the nonionic surfactant class.

If the surfactant molecule carries a negative charge when it is dissolved or dispersed in water, the surfactant is classified as anionic. Anionic surfactants include carboxylates such as soaps, acyl lactylates, acyl amides of amino acids, esters of sulfuric acid such as alkyl sulfates and ethoxylated alkyl sulfates, sulfonates such as alkyl benzene sulfonates, acyl isethionates, acyl taurates and sulfosuccinates, and phosphates. The most important members of the anionic surfactant class are the alkyl sulfates and the soaps.

If the surfactant molecule carries a positive charge when it is dissolved or dispersed in water, the surfactant is classified as cationic. Cationic surfactants include quaternary ammonium salts and ethoxylated amines. The quaternary ammonium salts are the most used members of this class.

If the surfactant molecule has the ability to carry either a positive or negative charge, the surfactant is classified as amphoteric. Amphoteric surfactants include acrylic acid derivatives, substituted alkylamides, N-alkylbetaines and phosphatides.

The use of surfactants in drug products, formulations and in emulsions has been reviewed (Rieger, in Pharmaceutical Dosage Forms, Marcel Dekker, Inc., New York, N.Y., 1988, p. 285).

Penetration Enhancers

In one embodiment, the present invention employs various penetration enhancers to accomplish the efficient delivery of nucleic acids, particularly oligonucleotides, to the skin of animals. Most drugs are present in solution in both ionized and nonionized forms. However, usually only lipid soluble or lipophilic drugs readily cross cell membranes. It has been discovered that even non-lipophilic drugs may cross cell membranes if the membrane to be crossed is treated with a penetration enhancer. In addition to aiding the diffusion of non-lipophilic drugs across cell membranes, penetration enhancers also enhance the permeability of lipophilic drugs.

Penetration enhancers may be classified as belonging to one of five broad categories, i.e., surfactants, fatty acids, bile salts, chelating agents, and non-chelating non-surfactants (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p. 92). Each of the above mentioned classes of penetration enhancers are described below in greater detail.

Surfactants

In connection with the present invention, surfactants (or "surface-active agents") are chemical entities which, when dissolved in an aqueous solution, reduce the surface tension of the solution or the interfacial tension between the aqueous solution and another liquid, with the result that absorption of oligonucleotides through the mucosa is enhanced. In addition to bile salts and fatty acids, these penetration enhancers include, for example, sodium lauryl sulfate, polyoxyethylene-9-lauryl ether and polyoxyethylene-20-cetyl ether) (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p. 92); and perfluorochemical emulsions, such as FC-43. Takahashi et al., J. Pharm. Pharmacol., 1988, 40, 252).

Fatty Acids

Various fatty acids and their derivatives which act as penetration enhancers include, for example, oleic acid, lauric acid, capric acid (n-decanoic acid), myristic acid, palmitic acid, stearic acid, linoleic acid, linolenic acid, dicaprate, tricaprate, monoolein (1-monooleoyl-rac-glycerol), dilaurin, caprylic acid, arachidonic acid, glycerol 1-monocaprate, 1-dodecylazacycloheptan-2-one, acylcarnitines, acylcholines, C.sub.1-10 alkyl esters thereof (e.g., methyl, isopropyl and t-butyl), and mono- and di-glycerides thereof (i.e., oleate, laurate, caprate, myristate, palmitate, stearate, linoleate, etc.) (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p. 92; Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33; El Hariri et al., J. Pharm. Pharmacol., 1992, 44, 651-654).

Bile Salts

The physiological role of bile includes the facilitation of dispersion and absorption of lipids and fat-soluble vitamins (Brunton, Chapter 38 in: Goodman & Gilman's The Pharmacological Basis of Therapeutics, 9th Ed., Hardman et al. Eds., McGraw-Hill, New York, 1996, pp. 934-935). Various natural bile salts, and their synthetic derivatives, act as penetration enhancers. Thus the term "bile salts" includes any of the naturally occurring components of bile as well as any of their synthetic derivatives. The bile salts of the invention include, for example, cholic acid (or its pharmaceutically acceptable sodium salt, sodium cholate), dehydrocholic acid (sodium dehydrocholate), deoxycholic acid (sodium deoxycholate), glucholic acid (sodium glucholate), glycholic acid (sodium glycocholate), glycodeoxycholic acid (sodium glycodeoxycholate), taurocholic acid (sodium taurocholate), taurodeoxycholic acid (sodium taurodeoxy-cholate), chenodeoxycholic acid (sodium chenodeoxy-cholate), ursodeoxycholic acid (UDCA), sodium tauro-24,25-dihydro-fusidate (STDHF), sodium glycodihydrofusidate and polyoxyethylene-9-lauryl ether (POE) (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, page 92; Swinyard, Chapter 39 In: Remington's Pharmaceutical Sciences, 18th Ed., Gennaro, ed., Mack Publishing Co., Easton, Pa., 1990, pages 782-783; Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33; Yamamoto et al., J. Pharm. Exp. Ther., 1992, 263, 25; Yamashita et al., J. Pharm. Sci., 1990, 79, 579-583).

Chelating Agents

Chelating agents, as used in connection with the present invention, can be defined as compounds that remove metallic ions from solution by forming complexes therewith, with the result that absorption of oligonucleotides through the mucosa is enhanced. With regards to their use as penetration enhancers in the present invention, chelating agents have the added advantage of also serving as DNase inhibitors, as most characterized DNA nucleases require a divalent metal ion for catalysis and are thus inhibited by chelating agents (Jarrett, J. Chromatogr., 1993, 618, 315-339). Chelating agents of the invention include but are not limited to disodium ethylenediaminetetraacetate (EDTA), citric acid, salicylates (e.g., sodium salicylate, 5-methoxysalicylate and homovanilate), N-acyl derivatives of collagen, laureth-9 and N-amino acyl derivatives of beta-diketones (enamines)(Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, page 92; Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33; Buur et al., J. Control Rel., 1990, 14, 43-51).

Non-Chelating Non-Surfactants

As used herein, non-chelating non-surfactant penetration enhancing compounds can be defined as compounds that demonstrate insignificant activity as chelating agents or as surfactants but that nonetheless enhance absorption of oligonucleotides through the alimentary mucosa (Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33). This class of penetration enhancers include, for example, unsaturated cyclic ureas, 1-alkyl- and 1-alkenylazacyclo-alkanone derivatives (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, page 92); and non-steroidal anti-inflammatory agents such as diclofenac sodium, indomethacin and phenylbutazone (Yamashita et al., J. Pharm. Pharmacol., 1987, 39, 621-626).

Agents that enhance uptake of oligonucleotides at the cellular level may also be added to the pharmaceutical and other compositions of the present invention. For example, cationic lipids, such as lipofectin (Junichi et al, U.S. Pat. No. 5,705,188), cationic glycerol derivatives, and polycationic molecules, such as polylysine (Lollo et al., PCT Application WO 97/30731), are also known to enhance the cellular uptake of oligonucleotides.

Other agents may be utilized to enhance the penetration of the administered nucleic acids, including glycols such as ethylene glycol and propylene glycol, pyrrols such as 2-pyrrol, azones, and terpenes such as limonene and menthone.

Carriers

Certain compositions of the present invention also incorporate carrier compounds in the formulation. As used herein, "carrier compound" or "carrier" can refer to a nucleic acid, or analog thereof, which is inert (i.e., does not possess biological activity per se) but is recognized as a nucleic acid by in vivo processes that reduce the bioavailability of a nucleic acid having biological activity by, for example, degrading the biologically active nucleic acid or promoting its removal from circulation. The coadministration of a nucleic acid and a carrier compound, typically with an excess of the latter substance, can result in a substantial reduction of the amount of nucleic acid recovered in the liver, kidney or other extracirculatory reservoirs, presumably due to competition between the carrier compound and the nucleic acid for a common receptor. For example, the recovery of a partially phosphorothioate oligonucleotide in hepatic tissue can be reduced when it is coadministered with polyinosinic acid, dextran sulfate, polycytidic acid or 4-acetamido-4'isothiocyano-stilbene-2,2'-disulfonic acid (Miyao et al., Antisense Res. Dev., 1995, 5, 115-121; Takakura et al., Antisense & Nucl. Acid Drug Dev., 1996, 6, 177-183).

Excipients

In contrast to a carrier compound, a "pharmaceutical carrier" or "excipient" is a pharmaceutically acceptable solvent, suspending agent or any other pharmacologically inert vehicle for delivering one or more nucleic acids to an animal. The excipient may be liquid or solid and is selected, with the planned manner of administration in mind, so as to provide for the desired bulk, consistency, etc., when combined with a nucleic acid and the other components of a given pharmaceutical composition. Typical pharmaceutical carriers include, but are not limited to, binding agents (e.g., pregelatinized maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose, etc.); fillers (e.g., lactose and other sugars, microcrystalline cellulose, pectin, gelatin, calcium sulfate, ethyl cellulose, polyacrylates or calcium hydrogen phosphate, etc.); lubricants (e.g., magnesium stearate, talc, silica, colloidal silicon dioxide, stearic acid, metallic stearates, hydrogenated vegetable oils, corn starch, polyethylene glycols, sodium benzoate, sodium acetate, etc.); disintegrants (e.g., starch, sodium starch glycolate, etc.); and wetting agents (e.g., sodium lauryl sulphate, etc.).

Pharmaceutically acceptable organic or inorganic excipient suitable for non-parenteral administration which do not deleteriously react with nucleic acids can also be used to formulate the compositions of the present invention. Suitable pharmaceutically acceptable carriers include, but are not limited to, water, salt solutions, alcohols, polyethylene glycols, gelatin, lactose, amylose, magnesium stearate, talc, silicic acid, viscous paraffin, hydroxymethylcellulose, polyvinylpyrrolidone and the like.

Formulations for topical administration of nucleic acids may include sterile and non-sterile aqueous solutions, non-aqueous solutions in common solvents such as alcohols, or solutions of the nucleic acids in liquid or solid oil bases. The solutions may also contain buffers, diluents and other suitable additives. Pharmaceutically acceptable organic or inorganic excipients suitable for non-parenteral administration which do not deleteriously react with nucleic acids can be used.

Suitable pharmaceutically acceptable excipients include, but are not limited to, water, salt solutions, alcohol, polyethylene glycols, gelatin, lactose, amylose, magnesium stearate, talc, silicic acid, viscous paraffin, hydroxymethylcellulose, polyvinylpyrrolidone and the like.

Other Components

The compositions of the present invention may additionally contain other adjunct components conventionally found in pharmaceutical compositions, at their art-established usage levels. Thus, for example, the compositions may contain additional, compatible, pharmaceutically-active materials such as, for example, antipruritics, astringents, local anesthetics or anti-inflammatory agents, or may contain additional materials useful in physically formulating various dosage forms of the compositions of the present invention, such as dyes, flavoring agents, preservatives, antioxidants, opacifiers, thickening agents and stabilizers. However, such materials, when added, should not unduly interfere with the biological activities of the components of the compositions of the present invention. The formulations can be sterilized and, if desired, mixed with auxiliary agents, e.g., lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, colorings, flavorings and/or aromatic substances and the like which do not deleteriously interact with the nucleic acid(s) of the formulation.

Aqueous suspensions may contain substances which increase the viscosity of the suspension including, for example, sodium carboxymethylcellulose, sorbitol and/or dextran. The suspension may also contain stabilizers.

Certain embodiments of the invention provide pharmaceutical compositions containing (a) one or more antisense compounds and (b) one or more other chemotherapeutic agents which function by a non-antisense mechanism. Examples of such chemotherapeutic agents include, but are not limited to, anticancer drugs such as daunorubicin, dactinomycin, doxorubicin, bleomycin, mitomycin, nitrogen mustard, chlorambucil, melphalan, cyclophosphamide, 6-mercaptopurine, 6-thioguanine, cytarabine (CA), 5-fluorouracil (5-FU), floxuridine (5-FUdR), methotrexate (MTX), colchicine, vincristine, vinblastine, etoposide, teniposide, cisplatin and diethylstilbestrol (DES). See, generally, The Merck Manual of Diagnosis and Therapy, 15th Ed., Berkow et al., eds., 1987, Rahway, N.J., pages 1206-1228). Anti-inflammatory drugs, including but not limited to nonsteroidal anti-inflammatory drugs and corticosteroids, and antiviral drugs, including but not limited to ribivirin, vidarabine, acyclovir and ganciclovir, may also be combined in compositions of the invention. See, generally, The Merck Manual of Diagnosis and Therapy, 15th Ed., Berkow et al., eds., 1987, Rahway, N.J., pages 2499-2506 and 46-49, respectively). Other non-antisense chemotherapeutic agents are also within the scope of this invention. Two or more combined compounds may be used together or sequentially.

In another related embodiment, compositions of the invention may contain one or more antisense compounds, particularly oligonucleotides, targeted to a first nucleic acid and one or more additional antisense compounds targeted to a second nucleic acid target. Numerous examples of antisense compounds are known in the art. Two or more combined compounds may be used together or sequentially.

The formulation of therapeutic compositions and their subsequent administration is believed to be within the skill of those in the art. Dosing is dependent on severity and responsiveness of the disease state to be treated, with the course of treatment lasting from several days to several months, or until a cure is effected or a diminution of the disease state is achieved. Optimal dosing schedules can be calculated from measurements of drug accumulation in the body of the patient. Persons of ordinary skill can easily determine optimum dosages, dosing methodologies and repetition rates. Optimum dosages may vary depending on the relative potency of individual oligonucleotides, and can generally be estimated based on EC.sub.50s found to be effective in in vitro and in vivo animal models. In general, dosage is from 0.01 .mu.g to 100 g per kg of body weight, and may be given once or more daily, weekly, monthly or yearly, or even once every 2 to 20 years. Persons of ordinary skill in the art can easily estimate repetition rates for dosing based on measured residence times and concentrations of the drug in bodily fluids or tissues. Following successful treatment, it may be desirable to have the patient undergo maintenance therapy to prevent the recurrence of the disease state, wherein the oligonucleotide is administered in maintenance doses, ranging from 0.01 .mu.g to 100 g per kg of body weight, once or more daily, to once every 20 years.

While the present invention has been described with specificity in accordance with certain of its preferred embodiments, the following examples serve only to illustrate the invention and are not intended to limit the same.

EXAMPLES

Example 1

Nucleoside Phosphoramidites for Oligonucleotide Synthesis Deoxy and 2'-alkoxy amidites

2'-Deoxy and 2'-methoxy beta-cyanoethyldiisopropyl phosphoramidites were purchased from commercial sources (e.g. Chemgenes, Needham, Mass. or Glen Research, Inc., Sterling, Va.). Other 2'-O-alkoxy substituted nucleoside amidites are prepared as described in U.S. Pat. No. 5,506,351, herein incorporated by reference. For oligonucleotides synthesized using 2'-alkoxy amidites, the standard cycle for unmodified oligonucleotides was utilized, except the wait step after pulse delivery of tetrazole and base was increased to 360 seconds.

Oligonucleotides containing 5-methyl-2'-deoxycytidine (5-Me-C) nucleotides were synthesized according to published methods [Sanghvi, et. al., Nucleic Acids Research, 1993, 21, 3197-3203] using commercially available phosphoramidites (Glen Research, Sterling, Va., or ChemGenes, Needham, Mass.).

2'-Fluoro amidites

2'-Fluorodeoxyadenosine amidites

2'-fluoro oligonucleotides were synthesized as described previously [Kawasaki, et. al., J. Med. Chem., 1993, 36, 831-841] and U.S. Pat. No. 5,670,633, herein incorporated by reference. Briefly, the protected nucleoside N6-benzoyl-2'-deoxy-2'-fluoroadenosine was synthesized utilizing commercially available 9-beta-D-arabinofuranosyladenine as starting material and by modifying literature procedures whereby the 2'-alpha-fluoro atom is introduced by a S.sub.N2-displacement of a 2'-beta-trityl group. Thus N6-benzoyl-9-beta-D-arabinofuranosyladenine was selectively protected in moderate yield as the 3',5'-ditetrahydropyranyl (THP) intermediate. Deprotection of the THP and N6-benzoyl groups was accomplished using standard methodologies and standard methods were used to obtain the 5'-dimethoxytrityl-(DMT) and 5'-DMT-3'-phosphoramidite intermediates.

2'-Fluorodeoxyguanosine

The synthesis of 2'-deoxy-2'-fluoroguanosine was accomplished using tetraisopropyldisiloxanyl (TPDS) protected 9-beta-D-arabinofuranosylguanine as starting material, and conversion to the intermediate diisobutyrylarabinofuranosylguanosine. Deprotection of the TPDS group was followed by protection of the hydroxyl group with THP to give diisobutyryl di-THP protected arabinofuranosylguanine. Selective O-deacylation and triflation was followed by treatment of the crude product with fluoride, then deprotection of the THP groups. Standard methodologies were used to obtain the 5'-DMT- and 5'-DMT-3'-phosphoramidites.

2'-Fluorouridine

Synthesis of 2'-deoxy-2'-fluorouridine was accomplished by the modification of a literature procedure in which 2,2'-anhydro-1-beta-D-arabinofuranosyluracil was treated with 70% hydrogen fluoride-pyridine. Standard procedures were used to obtain the 5'-DMT and 5'-DMT-3' phosphoramidites.

2'-Fluorodeoxycytidine

2'-deoxy-2'-fluorocytidine was synthesized via amination of 2'-deoxy-2'-fluorouridine, followed by selective protection to give N4-benzoyl-2'-deoxy-2'-fluorocytidine. Standard procedures were used to obtain the 5'-DMT and 5'-DMT-3' phosphoramidites.

2'-O-(2-Methoxyethyl) modified amidites

2'-O-Methoxyethyl-substituted nucleoside amidites are prepared as follows, or alternatively, as per the methods of Martin, P., Helvetica Chimica Acta, 1995, 78, 486-504.

2,2'-Anhydro[1-(beta-D-arabinofuranosyl)-5-methyluridine]

5-Methyluridine (ribosylthymine, commercially available through Yamasa, Choshi, Japan) (72.0 g, 0.279 M), diphenylcarbonate (90.0 g, 0.420 M) and sodium bicarbonate (2.0 g, 0.024 M) were added to DMF (300 mL). The mixture was heated to reflux, with stirring, allowing the evolved carbon dioxide gas to be released in a controlled manner. After 1 hour, the slightly darkened solution was concentrated under reduced pressure. The resulting syrup was poured into diethylether (2.5 L), with stirring. The product formed a gum. The ether was decanted and the residue was dissolved in a minimum amount of methanol (ca. 400 mL). The solution was poured into fresh ether (2.5 L) to yield a stiff gum. The ether was decanted and the gum was dried in a vacuum oven (60.degree. C. at 1 mm Hg for 24 h) to give a solid that was crushed to a light tan powder (57 g, 85% crude yield). The NMR spectrum was consistent with the structure, contaminated with phenol as its sodium salt (ca. 5%). The material was used as is for further reactions (or it can be purified further by column chromatography using a gradient of methanol in ethyl acetate (10-25%) to give a white solid, mp 222-4.degree. C.).

2'-O-Methoxyethyl-5-methyluridine

2,2'-Anhydro-5-methyluridine (195 g, 0.81 M), tris(2-methoxyethyl)borate (231 g, 0.98 M) and 2-methoxyethanol (1.2 L) were added to a 2 L stainless steel pressure vessel and placed in a pre-heated oil bath at 160.degree. C. After heating for 48 hours at 155-16 C., the vessel was opened and the solution evaporated to dryness and triturated with MeOH (200 mL). The residue was suspended in hot acetone (1 L). The insoluble salts were filtered, washed with acetone (150 mL) and the filtrate evaporated. The residue (280 g) was dissolved in CH.sub.3CN (600 mL) and evaporated. A silica gel column (3 kg) was packed in CH.sub.2Cl.sub.2/acetone/MeOH (20:5:3) containing 0.5% Et.sub.3NH. The residue was dissolved in CH.sub.2Cl.sub.2 (250 mL) and adsorbed onto silica (150 g) prior to loading onto the column. The product was eluted with the packing solvent to give 160 g (63%) of product. Additional material was obtained by reworking impure fractions.

2'O-Methoxyethyl-5'-O-dimethoxytrityl-5-methyluridine

2'-O-Methoxyethyl-5-methyluridine (160 g, 0.506 M) was co-evaporated with pyridine (250 mL) and the dried residue dissolved in pyridine (1.3 L). A first aliquot of dimethoxytrityl chloride (94.3 g, 0.278 M) was added and the mixture stirred at room temperature for one hour. A second aliquot of dimethoxytrityl chloride (94.3 g, 0.278 M) was added and the reaction stirred for an additional one hour. Methanol (170 mL) was then added to stop the reaction. HPLC showed the presence of approximately 70% product. The solvent was evaporated and triturated with CH.sub.3CN (200 mL). The residue was dissolved in CHCl.sub.3 (1.5 L) and extracted with 2.times.500 mL of saturated NaHCO.sub.3 and 2.times.500 mL of saturated NaCl. The organic phase was dried over Na.sub.2SO.sub.4, filtered and evaporated. 275 g of residue was obtained. The residue was purified on a 3.5 kg silica gel column, packed and eluted with EtOAc/hexane/acetone (5:5:1) containing 0.5% Et.sub.3NH. The pure fractions were evaporated to give 164 g of product. Approximately 20 g additional was obtained from the impure fractions to give a total yield of 183 g (57%).

3'-O-Acetyl-2'-O-methoxyethyl-5'-O-dimethoxytrityl-5-methyluridine

2'-O-Methoxyethyl-5'-O-dimethoxytrityl-5-methyluridine (106 g, 0.167 M), DMF/pyridine (750 mL of a 3:1 mixture prepared from 562 mL of DMF and 188 mL of pyridine) and acetic anhydride (24.38 mL, 0.258 M) were combined and stirred at room temperature for 24 hours. The reaction was monitored by TLC by first quenching the TLC sample with the addition of MeOH. Upon completion of the reaction, as judged by TLC, MeOH (50 mL) was added and the mixture evaporated at 35 C. The residue was dissolved in CHCl.sub.3 (800 mL) and extracted with 2.times.200 mL of saturated sodium bicarbonate and 2.times.200 mL of saturated NaCl. The water layers were back extracted with 200 mL of CHCl.sub.3. The combined organics were dried with sodium sulfate and evaporated to give 122 g of residue (approx. 90% product). The residue was purified on a 3.5 kg silica gel column and eluted using EtOAc/hexane (4:1). Pure product fractions were evaporated to yield 96 g (84%). An additional 1.5 g was recovered from later fractions.

3'-O-Acetyl-2'-O-methoxyethyl-5'-O-dimethoxytrityl-5-methyl-4-triazoleurid- ine

A first solution was prepared by dissolving 3'-O-acetyl-2'-O-methoxyethyl-5'-O-dimethoxytrityl-5-methyluridine (96 g, 0.144 M) in CH.sub.3CN (700 mL) and set aside. Triethylamine (189 mL, 1.44 M) was added to a solution of triazole (90 g, 1.3 M) in CH.sub.3CN (1 L), cooled to -5.degree. C. and stirred for 0.5 h using an overhead stirrer. POCl.sub.3 was added dropwise, over a 30 minute period, to the stirred solution maintained at 0-10.degree. C., and the resulting mixture stirred for an additional 2 hours. The first solution was added dropwise, over a 45 minute period, to the latter solution. The resulting reaction mixture was stored overnight in a cold room. Salts were filtered from the reaction mixture and the solution was evaporated. The residue was dissolved in EtOAc (1 L) and the insoluble solids were removed by filtration. The filtrate was washed with 1.times.300 mL of NaHCO.sub.3 and 2.times.300 mL of saturated NaCl, dried over sodium sulfate and evaporated. The residue was triturated with EtOAc to give the title compound.

2'-O-Methoxyethyl-5'-O-dimethoxytrityl-5-methylcytidine

A solution of 3'-O-acetyl-2'-O-methoxyethyl-5'-O-dimethoxytrityl-5-methyl-4-triazoleuri- dine (103 g, 0.141 M) in dioxane (500 mL) and NH.sub.4OH (30 mL) was stirred at room temperature for 2 hours. The dioxane solution was evaporated and the residue azeotroped with MeOH (2.times.200 mL). The residue was dissolved in MeOH (300 mL) and transferred to a 2 L stainless steel pressure vessel. MeOH (400 mL) saturated with NH.sub.3 gas was added and the vessel heated to 100.degree. C. for 2 hours (TLC showed complete conversion). The vessel contents were evaporated to dryness and the residue was dissolved in EtOAc (500 mL) and washed once with saturated NaCl (200 mL). The organics were dried over sodium sulfate and the solvent was evaporated to give 85 g (95%) of the title compound.

N4-Benzoyl-2'-O-methoxyethyl-5'-O-dimethoxytrityl-5-methylcytidine

2'-O-Methoxyethyl-5'-O-dimethoxytrityl-5-methylcytidine (85 g, 0.134 M) was dissolved in DMF (800 mL) and benzoic anhydride (37.2 g, 0.165 M) was added with stirring. After stirring for 3 hours, TLC showed the reaction to be approximately 95% complete. The solvent was evaporated and the residue azeotroped with MeOH (200 mL). The residue was dissolved in CHCl.sub.3 (700 mL) and extracted with saturated NaHCO.sub.3 (2.times.300 mL) and saturated NaCl (2.times.300 mL), dried over MgSO.sub.4 and evaporated to give a residue (96 g). The residue was chromatographed on a 1.5 kg silica column using EtOAc/hexane (1:1) containing 0.5% Et.sub.3NH as the eluting solvent. The pure product fractions were evaporated to give 90 g (90%) of the title compound.

N4-Benzoyl-2'-O-methoxyethyl-5'-O-dimethoxytrityl-5-methylcytidine-3'-amid- ite

N4-Benzoyl-2'-O-methoxyethyl-5'-O-dimethoxytrityl-5-methylcytidine (74 g, 0.10 M) was dissolved in CH.sub.2Cl.sub.2 (1 L). Tetrazole diisopropylamine (7.1 g) and 2-cyanoethoxy-tetra(isopropyl)-phosphite (40.5 mL, 0.123 M) were added with stirring, under a nitrogen atmosphere. The resulting mixture was stirred for 20 hours at room temperature (TLC showed the reaction to be 95% complete). The reaction mixture was extracted with saturated NaHCO.sub.3 (1.times.300 mL) and saturated NaCl (3.times.300 mL). The aqueous washes were back-extracted with CH.sub.2Cl.sub.2 (300 mL), and the extracts were combined, dried over MgSO.sub.4 and concentrated. The residue obtained was chromatographed on a 1.5 kg silica column using EtOAc/hexane (3:1) as the eluting solvent. The pure fractions were combined to give 90.6 g (87%) of the title compound.

2'-O-(Aminooxyethyl) nucleoside amidites and 2'-O-(dimethylaminooxyethyl) nucleoside amidites

2'-(Dimethylaminooxyethoxy) nucleoside amidites

2'-(Dimethylaminooxyethoxy) nucleoside amidites (also known in the art as 2'-O -(dimethylaminooxyethyl) nucleoside amidites) are prepared as described in the following paragraphs. Adenosine, cytidine and guanosine nucleoside amidites are prepared similarly to the thymidine (5-methyluridine) except the exocyclic amines are protected with a benzoyl moiety in the case of adenosine and cytidine and with isobutyryl in the case of guanosine.

5'-O-tert-Butyldiphenylsilyl-O.sup.2-2'-anhydro-5-methyluridine

O.sup.2-2'-anhydro-5-methyluridine (Pro. Bio. Sint., Varese, Italy, 100.0 g, 0.416 mmol), dimethylaminopyridine (0.66 g, 0.013 eq, 0.0054 mmol) were dissolved in dry pyridine (500 ml) at ambient temperature under an argon atmosphere and with mechanical stirring. tert-Butyldiphenylchlorosilane (125.8 g, 119.0 mL, 1.1 eq, 0.458 mmol) was added in one portion. The reaction was stirred for 16 h at ambient temperature. TLC (Rf 0.22, ethyl acetate) indicated a complete reaction. The solution was concentrated under reduced pressure to a thick oil. This was partitioned between dichloromethane (1 L) and saturated sodium bicarbonate (2.times.1 L) and brine (1 L). The organic layer was dried over sodium sulfate and concentrated under reduced pressure to a thick oil. The oil was dissolved in a 1:1 mixture of ethyl acetate and ethyl ether (600 mL) and the solution was cooled to -10.degree. C. The resulting crystalline product was collected by filtration, washed with ethyl ether (3.times.200 mL) and dried (40.degree. C., 1 mm Hg, 24 h) to 149 g (74.8%) of white solid. TLC and NMR were consistent with pure product.

5'-O-tert-Butyldiphenylsilyl-2'-O-(2-hydroxyethyl)-5-methyluridine

In a 2 L stainless steel, unstirred pressure reactor was added borane in tetrahydrofuran (1.0 M, 2.0 eq, 622 mL). In the fume hood and with manual stirring, ethylene glycol (350 mL, excess) was added cautiously at first until the evolution of hydrogen gas subsided. 5'-O-tert-Butyldiphenylsilyl-O.sup.2-2'-anhydro-5-methyluridine (149 g, 0.311 mol) and sodium bicarbonate (0.074 g, 0.003 eq) were added with manual stirring. The reactor was sealed and heated in an oil bath until an internal temperature of 160.degree. C. was reached and then maintained for 16 h (pressure<100 psig). The reaction vessel was cooled to ambient and opened. TLC(Rf 0.67 for desired product and Rf 0.82 for ara-T side product, ethyl acetate) indicated about 70% conversion to the product. In order to avoid additional side product formation, the reaction was stopped, concentrated under reduced pressure (10 to 1 mm Hg) in a warm water bath (40-100.degree. C.) with the more extreme conditions used to remove the ethylene glycol. Alternatively, once the low boiling solvent is gone, the remaining solution can be partitioned between ethyl acetate and water. The product will be in the organic phase. The residue was purified by column chromatography (2 kg silica gel, ethyl acetate-hexanes gradient 1:1 to 4:1). The appropriate fractions were combined, stripped and dried to product as a white crisp foam (84 g, 50%), contaminated starting material (17.4 g) and pure reusable starting material 20 g. The yield based on starting material less pure recovered starting material was 58%. TLC and NMR were consistent with 99% pure product.

2'-O-([2-phthaliamidoxy)ethyl]-5'-t-butyldiphenylsilyl-5-methyluridine

5'-O-tert-Butyldiphenylsilyl-2'-O-(2-hydroxyethyl)-5-methyluridine (20 g, 36.98 mmol) was mixed with triphenylphosphine (11.63 g, 44.36 mmol) and N-hydroxyphthalimide (7.24 g, 44.36 mmol). It was then dried over P.sub.2O.sub.5 under high vacuum for two days at 40.degree. C. The reaction mixture was flushed with argon and dry THF (369.8 mL, Aldrich, sure seal bottle) was added to get a clear solution. Diethyl-azodicarboxylate (6.98 mL, 44.36 mmol) was added dropwise to the reaction mixture. The rate of addition is maintained such that resulting deep red coloration is just discharged before adding the next drop. After the addition was complete, the reaction was stirred for 4 hrs. By that time TLC showed the completion of the reaction (ethylacetate:hexane, 60:40). The solvent was evaporated in vacuum. Residue obtained was placed on a flash column and eluted with ethyl acetate:hexane (60:40), to get 2'-O-([2-phthalimidoxy)ethyl]-5'-t-butyldiphenyl-silyl-5-methyluridine as white foam (21.819 g, 86%).

5'-O-tert-butyldiphenylsilyl-2'-O-[(2-formadoximinooxy)ethyl]-5-methylurid- ine

2'-O-([2-phthalimidoxy)ethyl]-5'-t-butyldiphenyl-silyl-5-methyluridine (3.1 g, 4.5 mmol) was dissolved in dry CH.sub.2Cl.sub.2 4.5 mL) and methylhydrazine (300 mL, 4.64 mmol) was added dropwise at -10.degree. C. to 0.degree. C. After 1 h the mixture was filtered, the filtrate was washed with ice cold CH.sub.2Cl.sub.2 and the combined organic phase was washed with water, brine and dried over anhydrous Na.sub.2SO.sub.4. The solution was concentrated to get 2'-O-(aminooxyethyl)thymidine, which was then dissolved in MeOH (67.5 mL). To this formaldehyde (20% aqueous solution, w/w, 1.1 eq.) was added and the resulting mixture was stirred for 1 h. Solvent was removed under vacuum; residue chromatographed to get 5'-O-tert-butyldiphenylsilyl-2'-O-[(2-formadoximi-nooxy)ethyl]-5-methylur- idine as white foam (1.95 g, 78%).

5'-O-tert-Butyldiphenylsilyl-2'-O--[N,N-dimethylaminooxyethyl]-5-methyluri- dine

5'-O-tert-butyldiphenylsilyl-2'-O-[(2-formadoximinooxy)ethyl]-5-methyluri- dine (1.77 g, 3.12 mmol) was dissolved in a solution of 1M pyridinium p-toluenesulfonate (PPTS) in dry MeOH (30.6 mL). Sodium cyanoborohydride (0.39 g, 6.13 mmol) was added to this solution at 10.degree. C. under inert atmosphere. The reaction mixture was stirred for 10 minutes at 10.degree. C. After that the reaction vessel was removed from the ice bath and stirred at room temperature for 2 h, the reaction monitored by TLC (5% MeOH in CH.sub.2Cl.sub.2). Aqueous NaHCO.sub.3 solution (5%, 10 mL) was added and extracted with ethyl acetate (2.times.20 mL). Ethyl acetate phase was dried over anhydrous Na.sub.2SO.sub.4, evaporated to dryness. Residue was dissolved in a solution of 1M PPTS in MeOH (30.6 mL). Formaldehyde (20% w/w, 30 mL, 3.37 mmol) was added and the reaction mixture was stirred at room temperature for 10 minutes. Reaction mixture cooled to 10.degree. C. in an ice bath, sodium cyanoborohydride (0.39 g, 6.13 mmol) was added and reaction mixture stirred at 10 C. for 10 minutes. After 10 minutes, the reaction mixture was removed from the ice bath and stirred at room temperature for 2 hrs. To the reaction mixture 5% NaHCO.sub.3 (25 mL) solution was added and extracted with ethyl acetate (2.times.25 mL). Ethyl acetate layer was dried over anhydrous Na.sub.2SO.sub.4 and evaporated to dryness. The residue obtained was purified by flash column chromatography and eluted with 5% MeOH in CH.sub.2Cl.sub.2 to get 5'-O-tert-butyldiphenylsilyl-2'-O--[N,N-dimethylamino-oxyethyl]-5-methylu- ridine as a white foam (14.6 g, 80%).

2'-O-(dimethylaminooxyethyl)-5-methyluridine

Triethylamine trihydrofluoride (3.91 mL, 24.0 mmol) was dissolved in dry THF and triethylamine (1.67 mL, 12 mmol, dry, kept over KOH). This mixture of triethylamine-2HF was then added to 5'-O-tert-butyldiphenylsilyl-2'-O--[N,N-dimethylaminooxyethyl]-5-methylur- idine (1.40 g, 2.4 mmol) and stirred at room temperature for 24 hrs. Reaction was monitored by TLC (5% MeOH in CH.sub.2Cl.sub.2). Solvent was removed under vacuum and the residue placed on a flash column and eluted with 10% MeOH in CH.sub.2Cl.sub.2 to get 2'-O-(dimethylaminooxyethyl)-5-methyluridine (766 mg, 92.5%).

5'-O-DMT-2'-O-(dimethylaminooxyethyl)-5-methyluridine

2'-O-(dimethylaminooxyethyl)-5-methyluridine (750 mg, 2.17 mmol) was dried over P.sub.2O.sub.5 under high vacuum overnight at 40.degree. C. It was then co-evaporated with anhydrous pyridine (20 mL). The residue obtained was dissolved in pyridine (11 mL) under argon atmosphere. 4-dimethylaminopyridine (26.5 mg, 2.60 mmol), 4,4'-dimethoxytrityl chloride (880 mg, 2.60 mmol) was added to the mixture and the reaction mixture was stirred at room temperature until all of the starting material disappeared. Pyridine was removed under vacuum and the residue chromatographed and eluted with 10% MeOH in CH.sub.2Cl.sub.2 (containing a few drops of pyridine) to get 5'-O-DMT-2'-O-(dimethylamino-oxyethyl)-5-methyluridine (1.13 g, 80%).

5'-O-DMT-2'-O-(2-N,N-dimethylaminooxyethyl)-5-methyluridine-3'-[(2-cyanoet- hyl)-N,N-diisopropylphosphoramidite]

5'-O-DMT-2'-O-(dimethylaminooxyethyl)-5-methyluridine (1.08 g, 1.67 mmol) was co-evaporated with toluene (20 mL). To the residue N,N-diisopropylamine tetrazonide (0.29 g, 1.67 mmol) was added and dried over P.sub.2O.sub.5 under high vacuum overnight at 40.degree. C. Then the reaction mixture was dissolved in anhydrous acetonitrile (8.4 mL) and 2-cyanoethyl-N,N,N.sup.1,N.sup.1-tetraisopropylphosphoramidite (2.12 mL, 6.08 mmol) was added. The reaction mixture was stirred at ambient temperature for 4 hrs under inert atmosphere. The progress of the reaction was monitored by TLC (hexane:ethyl acetate 1:1). The solvent was evaporated, then the residue was dissolved in ethyl acetate (70 mL) and washed with 5% aqueous NaHCO.sub.3 (40 mL). Ethyl acetate layer was dried over anhydrous Na.sub.2SO.sub.4 and concentrated. Residue obtained was chromatographed (ethyl acetate as eluent) to get 5'-O-DMT-2'-O-(2-N,N-dimethylaminooxyethyl)-5-methyluridine-3'-[(2-cyanoe- thyl)-N,N-diisopropylphosphoramidite] as a foam (1.04 g, 74.9%).

2'-(Aminooxyethoxy) nucleoside amidites

2'-(Aminooxyethoxy) nucleoside amidites (also known in the art as 2'-O-(aminooxyethyl) nucleoside amidites) are prepared as described in the following paragraphs. Adenosine, cytidine and thymidine nucleoside amidites are prepared similarly.

N2-isobutyryl-6-O-diphenylcarbamoyl-2'-O-(2-ethylacetyl)-5'-O-(4,4'-dimeth- oxytrityl)guanosine-3'-[(2-cyanoethyl)-N,N-diisopropylphosphoramidite]

The 2'-O-aminooxyethyl guanosine analog may be obtained by selective 2'-O-alkylation of diaminopurine riboside. Multigram quantities of diaminopurine riboside may be purchased from Schering AG (Berlin) to provide 2'-O-(2-ethylacetyl)diaminopurine riboside along with a minor amount of the 3'-O-isomer. 2'-O-(2-ethylacetyl) diaminopurine riboside may be resolved and converted to 2'-O-(2-ethylacetyl)guanosine by treatment with adenosine deaminase. (PCT Publication WO 94/02501). Standard protection procedures should afford 2'-O-(2-ethylacetyl)-5'-O-(4,4'-dimethoxy-trityl)guanosine and 2-N-isobutyryl-6-O-diphenylcarbamoyl-2'-O-(2-ethylacetyl)-5'-O-(4,4'-dime- thoxytrityl)guanosine which may be reduced to provide 2-N-isobutyryl-6-O- diphenylcarbamoyl-2'-O-(2-ethylacetyl)-5'-O-(4,4'-dimethoxytrityl)guanosi- ne. As before the hydroxyl group may be displaced by N-hydroxyphthalimide via a Mitsunobu reaction, and the protected nucleoside may phosphitylated as usual to yield 2-N-isobutyryl-6-O-diphenylcarbamoyl-2'-O-(2-ethylacetyl)-5'-O-(4,4'-dime- thoxytrityl)guanosine-3'-[(2-cyanoethyl)-N,N-diisopropylphosphoramidite].

2'-dimethylaminoethoxyethoxy (2'-DMAEOE) nucleoside amidites

2'-dimethylaminoethoxyethoxy nucleoside amidites (also known in the art as 2'-O- dimethylaminoethoxyethyl, i.e., 2'-O--CH.sub.2--O--CH.sub.2--N(CH.sub.2).sub.2, or 2'-DMAEOE nucleoside amidites) are prepared as follows. Other nucleoside amidites are prepared similarly.

2'-O-[2(2-N,N-dimethylaminoethoxy)ethyl]-5-methyl uridine

2[2-(Dimethylamino)ethoxy]ethanol (Aldrich, 6.66 g, 50 mmol) is slowly added to a solution of borane in tetrahydrofuran (1 M, 10 mL, 10 mmol) with stirring in a 100 mL bomb. Hydrogen gas evolves as the solid dissolves. O.sup.2-,2'-anhydro-5-methyluridine (1.2 g, 5 mmol), and sodium bicarbonate (2.5 mg) are added and the bomb is sealed, placed in an oil bath and heated to 155.degree. C. for 26 hours. The bomb is cooled to room temperature and opened. The crude solution is concentrated and the residue partitioned between water (200 mL) and hexanes (200 mL). The excess phenol is extracted into the hexane layer. The aqueous layer is extracted with ethyl acetate (3.times.200 mL) and the combined organic layers are washed once with water, dried over anhydrous sodium sulfate and concentrated. The residue is columned on silica gel using methanol/methylene chloride 1:20 (which has 2% triethylamine) as the eluent. As the column fractions are concentrated a colorless solid forms which is collected to give the title compound as a white solid.

5'-O-dimethoxytrityl-2'-O-[2(2-N,N-dimethylaminoethoxy)ethyl)]-5-methyl uridine

To 0.5 g (1.3 mmol) of 2'-O-[2(2-N,N-dimethylaminoethoxy)ethyl)]-5-methyl uridine in anhydrous pyridine (8 mL), triethylamine (0.36 mL) and dimethoxytrityl chloride (DMT-Cl, 0.87 g, 2 eq.) are added and stirred for 1 hour. The reaction mixture is poured into water (200 mL) and extracted with CH.sub.2Cl.sub.2 (2.times.200 mL). The combined CH.sub.2Cl.sub.2 layers are washed with saturated NaHCO.sub.3 solution, followed by saturated NaCl solution and dried over anhydrous sodium sulfate. Evaporation of the solvent followed by silica gel chromatography using MeOH:CH.sub.2Cl.sub.2:Et.sub.3N (20:1, v/v, with 1% triethylamine) gives the title compound.

5'-O-Dimethoxytrityl-2'-O-[2(2-N,N-dimethylamino-ethoxy)ethyl)]-5-methyl uridine-3'-O-(cyanoethyl-N,N-diisopropyl)phosphoramidite

Diisopropylaminotetrazolide (0.6 g) and 2-cyanoethoxy-N,N-diisopropyl phosphoramidite (1.1 mL, 2 eq.) are added to a solution of 5'-O-dimethoxytrityl-2'-O-[2(2-N,N-dimethylamino-ethoxy)ethyl)]-5-methylu- ridine (2.17 g, 3 mmol) dissolved in CH.sub.2Cl.sub.2 (20 mL) under an atmosphere of argon. The reaction mixture is stirred overnight and the solvent evaporated. The resulting residue is purified by silica gel flash column chromatography with ethyl acetate as the eluent to give the title compound.

Example 2

Oligonucleotide Synthesis

Unsubstituted and substituted phosphodiester (P.dbd.O) oligonucleotides are synthesized on an automated DNA synthesizer (Applied Biosystems model 380B) using standard phosphoramidite chemistry with oxidation by iodine.

Phosphorothioates (P.dbd.S) are synthesized as for the phosphodiester oligonucleotides except the standard oxidation bottle was replaced by 0.2 M solution of 3H-1,2-benzodithiole-3-one 1,1-dioxide in acetonitrile for the stepwise thiation of the phosphite linkages. The thiation wait step was increased to 68 sec and was followed by the capping step. After cleavage from the CPG column and deblocking in concentrated ammonium hydroxide at 55 C. (18 h), the oligonucleotides were purified by precipitating twice with 2.5 volumes of ethanol from a 0.5 M NaCl solution. Phosphinate oligonucleotides are prepared as described in U.S. Pat. No. 5,508,270, herein incorporated by reference.

Alkyl phosphonate oligonucleotides are prepared as described in U.S. Pat. No. 4,469,863, herein incorporated by reference.

3'-Deoxy-3'-methylene phosphonate oligonucleotides are prepared as described in U.S. Pat. No. 5,610,289 or 5,625,050, herein incorporated by reference.

Phosphoramidite oligonucleotides are prepared as described in U.S. Pat. No. 5,256,775 or U.S. Pat. No. 5,366,878, herein incorporated by reference.

Alkylphosphonothioate oligonucleotides are prepared as described in PCT applications PCT/US94/00902 and PCT/US93/06976 (published as WO 94/17093 and WO 94/02499, respectively), herein incorporated by reference.

3'-Deoxy-3'-amino phosphoramidate oligonucleotides are prepared as described in U.S. Pat. No. 5,476,925, herein incorporated by reference.

Phosphotriester oligonucleotides are prepared as described in U.S. Pat. No. 5,023,243, herein incorporated by reference.

Borano phosphate oligonucleotides are prepared as described in U.S. Pat. Nos. 5,130,302 and 5,177,198, both herein incorporated by reference.

Example 3

Oligonucleoside Synthesis

Methylenemethylimino linked oligonucleosides, also identified as MMI linked oligonucleosides, methylenedimethylhydrazo linked oligonucleosides, also identified as MDH linked oligonucleosides, and methylenecarbonylamino linked oligonucleosides, also identified as amide-3 linked oligonucleosides, and methyleneaminocarbonyl linked oligonucleosides, also identified as amide-4 linked oligonucleosides, as well as mixed backbone compounds having, for instance, alternating MMI and P.dbd.O or P.dbd.S linkages are prepared as described in U.S. Pat. Nos. 5,378,825; 5,386,023; 5,489,677; 5,602,240; and 5,610,289, all of which are herein incorporated by reference.

Formacetal and thioformacetal linked oligonucleosides are prepared as described in U.S. Pat. Nos. 5,264,562 and 5,264,564, herein incorporated by reference.

Ethylene oxide linked oligonucleosides are prepared as described in U.S. Pat. No. 5,223,618, herein incorporated by reference.

Example 4

PNA Synthesis

Peptide nucleic acids (PNAs) are prepared in accordance with any of the various procedures referred to in Peptide Nucleic Acids (PNA): Synthesis, Properties and Potential Applications, Bioorganic & Medicinal Chemistry, 1996, 4, 5-23. They may also be prepared in accordance with U.S. Pat. Nos. 5,539,082; 5,700,922; and 5,719,262, herein incorporated by reference.

Example 5

Synthesis of Chimeric Oligonucleotides

Chimeric oligonucleotides, oligonucleosides or mixed oligonucleotides/oligonucleosides of the invention can be of several different types. These include a first type wherein the "gap" segment of linked nucleosides is positioned between 5' and 3' "wing" segments of linked nucleosides and a second "open end" type wherein the "gap" segment is located at either the 3' or the 5' terminus of the oligomeric compound. Oligonucleotides of the first type are also known in the art as "gapmers" or gapped oligonucleotides. Oligonucleotides of the second type are also known in the art as "hemimers" or "wingmers".

[2'-O-Me]-[2'-deoxy]-[2'-O-Me]Chimeric Phosphorothioate Oligonucleotides

Chimeric oligonucleotides having 2'-O-alkyl phosphorothioate and 2'-deoxy phosphorothioate oligonucleotide segments are synthesized using an Applied Biosystems automated DNA synthesizer Model 380B, as above. Oligonucleotides are synthesized using the automated synthesizer and 2'-deoxy-5'-dimethoxytrityl-3'-O-phosphoramidite for the DNA portion and 5'-dimethoxytrityl-2'-O-methyl-3'-O-phosphoramidite for 5' and 3' wings. The standard synthesis cycle is modified by increasing the wait step after the delivery of tetrazole and base to 600 s repeated four times for RNA and twice for 2'-O-methyl. The fully protected oligonucleotide is cleaved from the support and the phosphate group is deprotected in 3:1 ammonia/ethanol at room temperature overnight then lyophilized to dryness. Treatment in methanolic ammonia for 24 hrs at room temperature is then done to deprotect all bases and sample was again lyophilized to dryness. The pellet is resuspended in 1M TBAF in THF for 24 hrs at room temperature to deprotect the 2' positions. The reaction is then quenched with 1M TEAA and the sample is then reduced to 1/2 volume by rotovac before being desalted on a G25 size exclusion column. The oligo recovered is then analyzed spectrophotometrically for yield and for purity by capillary electrophoresis and by mass spectrometry.

[2'-O-(2-Methoxyethyl)]-[2'-deoxy]-[2'-O-(Methoxyethyl)]Chimeric Phosphorothioate Oligonucleotides

[2'-O-(2-methoxyethyl)]-[2'-deoxy]-[-2'-O-(methoxyethyl)]chimeric phosphorothioate oligonucleotides were prepared as per the procedure above for the 2'-O-methyl chimeric oligonucleotide, with the substitution of 2'-O-(methoxyethyl)amidites for the 2'-O-methyl amidites.

[2'-O-(2-Methoxyethyl)Phosphodiester]-[2'-deoxy Phosphorothioate]-[2'-O-(2-Methoxyethyl)Phosphodiester]Chimeric Oligonucleotides

[2'-O-(2-methoxyethyl phosphodiester]-[2'-deoxy phosphorothioate]-[2'-O-(methoxyethyl)phosphodiester]chimeric oligonucleotides are prepared as per the above procedure for the 2'-O-methyl chimeric oligonucleotide with the substitution of 2'-O-(methoxyethyl)amidites for the 2'-O-methyl amidites, oxidization with iodine to generate the phosphodiester internucleotide linkages within the wing portions of the chimeric structures and sulfurization utilizing 3,H-1,2 benzodithiole-3-one 1,1 dioxide (Beaucage Reagent) to generate the phosphorothioate internucleotide linkages for the center gap.

Other chimeric oligonucleotides, chimeric oligonucleosides and mixed chimeric oligonucleotides/oligonucleosides are synthesized according to U.S. Pat. No. 5,623,065, herein incorporated by reference.

Example 6

Oligonucleotide Isolation

After cleavage from the controlled pore glass column (Applied Biosystems) and deblocking in concentrated ammonium hydroxide at 55.degree. C. for 18 hours, the oligonucleotides or oligonucleosides are purified by precipitation twice out of 0.5 M NaCl with 2.5 volumes ethanol. Synthesized oligonucleotides were analyzed by polyacrylamide gel electrophoresis on denaturing gels and judged to be at least 85% full length material. The relative amounts of phosphorothioate and phosphodiester linkages obtained in synthesis were periodically checked by .sup.31P nuclear magnetic resonance spectroscopy, and for some studies oligonucleotides were purified by HPLC, as described by Chiang et al., J. Biol. Chem. 1991, 266, 18162-18171. Results obtained with HPLC-purified material were similar to those obtained with non-HPLC purified material.

Example 7

Oligonucleotide Synthesis--96 Well Plate Format

Oligonucleotides were synthesized via solid phase P(III) phosphoramidite chemistry on an automated synthesizer capable of assembling 96 sequences simultaneously in a standard 96 well format. Phosphodiester internucleotide linkages were afforded by oxidation with aqueous iodine. Phosphorothioate internucleotide linkages were generated by sulfurization utilizing 3,H-1,2 benzodithiole-3-one 1,1 dioxide (Beaucage Reagent) in anhydrous acetonitrile. Standard base-protected beta-cyanoethyldiisopropyl phosphoramidites were purchased from commercial vendors (e.g. PE-Applied Biosystems, Foster City, Calif., or Pharmacia, Piscataway, N.J.). Non-standard nucleosides are synthesized as per known literature or patented methods. They are utilized as base protected beta-cyanoethyldiisopropyl phosphoramidites.

Oligonucleotides were cleaved from support and deprotected with concentrated NH.sub.4OH at elevated temperature (55-60.degree. C.) for 12-16 hours and the released product then dried in vacuo. The dried product was then re-suspended in sterile water to afford a master plate from which all analytical and test plate samples are then diluted utilizing robotic pipettors.

Example 8

Oligonucleotide Analysis--96 Well Plate Format

The concentration of oligonucleotide in each well was assessed by dilution of samples and UV absorption spectroscopy. The full-length integrity of the individual products was evaluated by capillary electrophoresis (CE) in either the 96 well format (Beckman P/ACE.TM. MDQ instrument) or, for individually prepared samples, on a commercial CE apparatus (e.g., Beckman P/ACE.TM. 5000 instrument, ABI 270 instrument). Base and backbone composition was confirmed by mass analysis of the compounds utilizing electrospray-mass spectroscopy. All assay test plates were diluted from the master plate using single and multi-channel robotic pipettors. Plates were judged to be acceptable if at least 85% of the compounds on the plate were at least 85% full length.

Example 9

Cell Culture and Oligonucleotide Treatment

The effect of antisense compounds on target nucleic acid expression can be tested in any of a variety of cell types provided that the target nucleic acid is present at measurable levels. This can be routinely determined using, for example, PCR or Northern blot analysis. The following 5 cell types are provided for illustrative purposes, but other cell types can be routinely used, provided that the target is expressed in the cell type chosen. This can be readily determined by methods routine in the art, for example Northern blot analysis, Ribonuclease protection assays, or RT-PCR.

T-24 Cells

The human transitional cell bladder carcinoma cell line T-24 was obtained from the American Type Culture Collection (ATCC) (Manassas, Va.). T-24 cells were routinely cultured in complete McCoy's 5A basal media (Gibco/Life Technologies, Gaithersburg, Md.) supplemented with 10% fetal calf serum (Gibco/Life Technologies, Gaithersburg, Md.), penicillin 100 units per mL, and streptomycin 100 .mu.g/mL (Gibco/Life Technologies, Gaithersburg, Md.). Cells were routinely passaged by trypsinization and dilution when they reached 90% confluence. Cells were seeded into 96-well plates (Falcon-Primaria #3872) at a density of 7000 cells/well for use in RT-PCR analysis.

For Northern blotting or other analysis, cells may be seeded onto 100 mm or other standard tissue culture plates and treated similarly, using appropriate volumes of medium and oligonucleotide.

A549 Cells

The human lung carcinoma cell line A549 was obtained from the American Type Culture Collection (ATCC) (Manassas, Va.). A549 cells were routinely cultured in DMEM basal media (Gibco/Life Technologies, Gaithersburg, Md.) supplemented with 10% fetal calf serum (Gibco/Life Technologies, Gaithersburg, Md.), penicillin 100 units per mL, and streptomycin 100 .mu.g/mL (Gibco/Life Technologies, Gaithersburg, Md.). Cells were routinely passaged by trypsinization and dilution when they reached 90% confluence.

NHDF Cells

Human neonatal dermal fibroblast (NHDF) were obtained from the Clonetics Corporation (Walkersville Md.). NHDFs were routinely maintained in Fibroblast Growth Medium (Clonetics Corporation, Walkersville, Md.) supplemented as recommended by the supplier. Cells were maintained for up to 10 passages as recommended by the supplier.

HEK Cells

Human embryonic keratinocytes (HEK) were obtained from the Clonetics Corporation (Walkersville, Md.). HEKs were routinely maintained in Keratinocyte Growth Medium (Clonetics Corporation, Walkersville Md.) formulated as recommended by the supplier. Cells were routinely maintained for up to 10 passages as recommended by the supplier.

PC-12 Cells

The rat neuronal cell line PC-12 was obtained from the American Type Culture Collection (Manassas, Va.). PC-12 cells were routinely cultured in DMEM, high glucose (Gibco/Life Technologies, Gaithersburg, Md.) supplemented with 10% horse serum+5% fetal calf serum (Gibco/Life Technologies, Gaithersburg, Md.). Cells were routinely passaged by trypsinization and dilution when they reached 90% confluence. Cells were seeded into 96-well plates (Falcon-Primaria #3872) at a density of 20000 cells/well for use in RT-PCR analysis.

For Northern blotting or other analysis, cells may be seeded onto 100 mm or other standard tissue culture plates and treated similarly, using appropriate volumes of medium and oligonucleotide.

Treatment with Antisense Compounds

When cells reached 80% confluency, they were treated with oligonucleotide. For cells grown in 96-well plates, wells were washed once with 200 .mu.l, OPTI-MEM.TM.-1 reduced-serum medium (Gibco BRL) and then treated with 130 .mu.l of OPTI-MEM.TM.-1 medium containing 3.75 .mu.g/mL LIPOFECTIN.TM. reagent (Gibco BRL) and the desired concentration of oligonucleotide. After 4-7 hours of treatment, the medium was replaced with fresh medium. Cells were harvested 16-24 hours after oligonucleotide treatment.

The concentration of oligonucleotide used varies from cell line to cell line. To determine the optimal oligonucleotide concentration for a particular cell line, the cells are treated with a positive control oligonucleotide at a range of concentrations. For human cells the positive control oligonucleotide is ISIS 13920, TCCGTCATCGCTCCTCAGGG, SEQ ID NO: 1, a 2'-O-methoxyethyl gapmer (2'-O-methoxyethyls shown in bold) with a phosphorothioate backbone which is targeted to human H-ras. For mouse or rat cells the positive control oligonucleotide is ISIS 15770, ATGCATTCTGCCCCCAAGGA, SEQ ID NO: 2, a 2'-O-methoxyethyl gapmer (2'-O-methoxyethyls shown in bold) with a phosphorothioate backbone which is targeted to both mouse and rat c-raf. The concentration of positive control oligonucleotide that results in 80% inhibition of c-Ha-ras (for ISIS 13920) or c-raf (for ISIS 15770) mRNA is then utilized as the screening concentration for new oligonucleotides in subsequent experiments for that cell line. If 80% inhibition is not achieved, the lowest concentration of positive control oligonucleotide that results in 60% inhibition of H-ras or c-raf mRNA is then utilized as the oligonucleotide screening concentration in subsequent experiments for that cell line. If 60% inhibition is not achieved, that particular cell line is deemed as unsuitable for oligonucleotide transfection experiments.

Example 10

Analysis of Oligonucleotide Inhibition of PTP1B Expression

Antisense modulation of PTP1B expression can be assayed in a variety of ways known in the art. For example, PTP1B mRNA levels can be quantitated by, e.g., Northern blot analysis, competitive polymerase chain reaction (PCR), or real-time PCR (RT-PCR). Real-time quantitative PCR is presently preferred. RNA analysis can be performed on total cellular RNA or poly(A)+ mRNA. Methods of RNA isolation are taught in, for example, Ausubel, F. M. et al., Current Protocols in Molecular Biology, Volume 1, pp. 4.1.1-4.2.9 and 4.5.1-4.5.3, John Wiley & Sons, Inc., 1993. Northern blot analysis is routine in the art and is taught in, for example, Ausubel, F. M. et al., Current Protocols in Molecular Biology, Volume 1, pp. 4.2.1-4.2.9, John Wiley & Sons, Inc., 1996. Real-time quantitative (PCR) can be conveniently accomplished using the commercially available ABI PRISM.TM. 7700 Sequence Detection System, available from PE-Applied Biosystems, Foster City, Calif. and used according to manufacturer's instructions. Prior to quantitative PCR analysis, primer-probe sets specific to the target gene being measured are evaluated for their ability to be "multiplexed" with a GAPDH amplification reaction. In multiplexing, both the target gene and the internal standard gene GAPDH are amplified concurrently in a single sample. In this analysis, mRNA isolated from untreated cells is serially diluted. Each dilution is amplified in the presence of primer-probe sets specific for GAPDH only, target gene only ("single-plexing"), or both (multiplexing). Following PCR amplification, standard curves of GAPDH and target mRNA signal as a function of dilution are generated from both the single-plexed and multiplexed samples. If both the slope and correlation coefficient of the GAPDH and target signals generated from the multiplexed samples fall within 10% of their corresponding values generated from the single-plexed samples, the primer-probe set specific for that target is deemed as multiplexable. Other methods of PCR are also known in the art.

Protein levels of PTP1B can be quantitated in a variety of ways well known in the art, such as immunoprecipitation, Western blot analysis (immunoblotting), ELISA or fluorescence-activated cell sorting (FACS). Antibodies directed to PTP1B can be identified and obtained from a variety of sources, such as the MSRS catalog of antibodies (Aerie Corporation, Birmingham, Mich.), or can be prepared via conventional antibody generation methods. Methods for preparation of polyclonal antisera are taught in, for example, Ausubel, F. M. et al., Current Protocols in Molecular Biology, Volume 2, pp. 11.12.1-11.12.9, John Wiley & Sons, Inc., 1997. Preparation of monoclonal antibodies is taught in, for example, Ausubel, F. M. et al., Current Protocols in Molecular Biology, Volume 2, pp. 11.4.1-11.11.5, John Wiley & Sons, Inc., 1997.

Immunoprecipitation methods are standard in the art and can be found at, for example, Ausubel, F. M. et al., Current Protocols in Molecular Biology, Volume 2, pp. 10.16.1-10.16.11, John Wiley & Sons, Inc., 1998. Western blot (immunoblot) analysis is standard in the art and can be found at, for example, Ausubel, F. M. et al., Current Protocols in Molecular Biology, Volume 2, pp. 10.8.1-10.8.21, John Wiley & Sons, Inc., 1997. Enzyme-linked immunosorbent assays (ELISA) are standard in the art and can be found at, for example, Ausubel, F. M. et al., Current Protocols in Molecular Biology, Volume 2, pp. 11.2.1-11.2.22, John Wiley & Sons, Inc., 1991.

Example 11

Poly(A)+ mRNA Isolation

Poly(A)+ mRNA was isolated according to Miura et al., Clin. Chem., 1996, 42, 1758-1764. Other methods for poly(A)+ mRNA isolation are taught in, for example, Ausubel, F. M. et al., Current Protocols in Molecular Biology, Volume 1, pp. 4.5.1-4.5.3, John Wiley & Sons, Inc., 1993. Briefly, for cells grown on 96-well plates, growth medium was removed from the cells and each well was washed with 200 .mu.L cold PBS. Sixty .mu.L lysis buffer (10 mM Tris-HCl, pH 7.6, 1 mM EDTA, 0.5 M NaCl, 0.5% NP-40, 20 mM vanadyl-ribonucleoside complex) was added to each well, the plate was gently agitated and then incubated at room temperature for five minutes. Fifty-five .mu.L of lysate was transferred to Oligo d(T) coated 96-well plates (AGCT Inc., Irvine Calif.). Plates were incubated for 60 minutes at room temperature, washed 3 times with 200 .mu.l of wash buffer (10 mM Tris-HCl pH 7.6, 1 mM EDTA, 0.3 M NaCl). After the final wash, the plate was blotted on paper towels to remove excess wash buffer and then air-dried for 5 minutes. 60 .mu.L of elution buffer (5 mM Tris-HCl pH 7.6), preheated to 70.degree. C. was added to each well, the plate was incubated on a 90.degree. C. hot plate for 5 minutes, and the eluate was then transferred to a fresh 96-well plate.

Cells grown on 100 mm or other standard plates may be treated similarly, using appropriate volumes of all solutions.

Example 12

Total RNA Isolation

Total mRNA was isolated using an RNEASY 96.TM. kit and buffers purchased from Qiagen Inc. (Valencia, Calif.) following the manufacturer's recommended procedures. Briefly, for cells grown on 96-well plates, growth medium was removed from the cells and each well was washed with 200 .mu.L cold PBS. One hundred .mu.L Buffer RLT was added to each well and the plate vigorously agitated for 20 seconds. One hundred .mu.L of 70% ethanol was then added to each well and the contents mixed by pipetting three times up and down. The samples were then transferred to the RNEASY 96.TM. well plate attached to a QIAVAC.TM. manifold fitted with a waste collection tray and attached to a vacuum source. Vacuum was applied for 15 seconds. One mL of Buffer RW1 was added to each well of the RNEASY 96.TM. plate and the vacuum again applied for 15 seconds. One mL of Buffer RPE was then added to each well of the RNEASY 96.TM. plate and the vacuum applied for a period of 15 seconds. The Buffer RPE wash was then repeated and the vacuum was applied for an additional 10 minutes. The plate was then removed from the QIAVAC.TM. manifold and blotted dry on paper towels. The plate was then re-attached to the QIAVAC.TM. manifold fitted with a collection tube rack containing 1.2 mL collection tubes. RNA was then eluted by pipetting 60 .mu.L, water into each well, incubating 1 minute, and then applying the vacuum for 30 seconds. The elution step was repeated with an additional 60 .mu.L water.

The repetitive pipetting and elution steps may be automated using a QIAGEN Bio-Robot 9604 apparatus (Qiagen, Inc., Valencia, Calif.). Essentially, after lysing of the cells on the culture plate, the plate is transferred to the robot deck where the pipetting, DNase treatment and elution steps are carried out.

Example 13

Real-Time Quantitative PCR Analysis of PTP1B mRNA Levels

Quantitation of PTP1B mRNA levels was determined by real-time quantitative PCR using the ABI PRISM.TM. 7700 Sequence Detection System (PE-Applied Biosystems, Foster City, Calif.) according to manufacturer's instructions. This is a closed-tube, non-gel-based, fluorescence detection system which allows high-throughput quantitation of polymerase chain reaction (PCR) products in real-time. As opposed to standard PCR, in which amplification products are quantitated after the PCR is completed, products in real-time quantitative PCR are quantitated as they accumulate. This is accomplished by including in the PCR reaction an oligonucleotide probe that anneals specifically between the forward and reverse PCR primers, and contains two fluorescent dyes. A reporter dye (e.g., JOE, FAM, or VIC, obtained from either Operon Technologies Inc., Alameda, Calif. or PE-Applied Biosystems, Foster City, Calif.) is attached to the 5' end of the probe and a quencher dye (e.g., TAMRA, obtained from either Operon Technologies Inc., Alameda, Calif. or PE-Applied Biosystems, Foster City, Calif.) is attached to the 3' end of the probe. When the probe and dyes are intact, reporter dye emission is quenched by the proximity of the 3' quencher dye. During amplification, annealing of the probe to the target sequence creates a substrate that can be cleaved by the 5'-exonuclease activity of Taq polymerase. During the extension phase of the PCR amplification cycle, cleavage of the probe by Taq polymerase releases the reporter dye from the remainder of the probe (and hence from the quencher moiety) and a sequence-specific fluorescent signal is generated. With each cycle, additional reporter dye molecules are cleaved from their respective probes, and the fluorescence intensity is monitored at regular intervals by laser optics built into the ABI PRISM.TM. 7700 Sequence Detection System. In each assay, a series of parallel reactions containing serial dilutions of mRNA from untreated control samples generates a standard curve that is used to quantitate the percent inhibition after antisense oligonucleotide treatment of test samples.

PCR reagents were obtained from PE-Applied Biosystems, Foster City, Calif. RT-PCR reactions were carried out by adding 25 .mu.L PCR cocktail (1.times. TAQMAN.TM. buffer A, 5.5 mM MgCl.sub.2, 300 .mu.M each of dATP, dCTP and dGTP, 600 .mu.M of dUTP, 100 nM each of forward primer, reverse primer, and probe, 20 Units RNAse inhibitor, 1.25 Units AMPLITAQ GOLD.TM. reagent, and 12.5 Units MuLV reverse transcriptase) to 96 well plates containing 25 .mu.L poly(A) mRNA solution. The RT reaction was carried out by incubation for 30 minutes at 48.degree. C. Following a 10 minute incubation at 95.degree. C. to activate the AMPLITAQ GOLD.TM. reagent, 40 cycles of a two-step PCR protocol were carried out: 95.degree. C. for 15 seconds (denaturation) followed by 60.degree. C. for 1.5 minutes (annealing/extension).

Probes and primers to human PTP1B were designed to hybridize to a human PTP1B sequence, using published sequence information (GenBank accession number M31724, incorporated herein as SEQ ID NO:3). For human PTP1B the PCR primers were:

forward primer: GGAGTTCGAGCAGATCGACAA (SEQ ID NO: 4)

reverse primer: GGCCACTCTACATGGGAAGTC (SEQ ID NO: 5) and the PCR probe was: FAM-AGCTGGGCGGCCATTTACCAGGAT-TAMRA

(SEQ ID NO: 6) where FAM (PE-Applied Biosystems, Foster City, Calif.) is the fluorescent reporter dye) and TAMRA (PE-Applied Biosystems, Foster City, Calif.) is the quencher dye. For human GAPDH the PCR primers were:

forward primer: GAAGGTGAAGGTCGGAGTC (SEQ ID NO: 7)

reverse primer: GAAGATGGTGATGGGATTTC (SEQ ID NO: 8) and the PCR probe was: 5' JOE-CAAGCTTCCCGTTCTCAGCC-TAMRA 3' (SEQ ID NO: 9) where JOE (PE-Applied Biosystems, Foster City, Calif.) is the fluorescent reporter dye) and TAMRA (PE-Applied Biosystems, Foster City, Calif.) is the quencher dye.

Probes and primers to rat PTP1B were designed to hybridize to a rat PTP1B sequence, using published sequence information (GenBank accession number M33962, incorporated herein as SEQ ID NO:10). For rat PTP1B the PCR primers were:

forward primer: CGAGGGTGCAAAGTTCATCAT (SEQ ID NO:11)

reverse primer: CCAGGTCTTCATGGGAAAGCT (SEQ ID NO: 12) and the PCR probe was: FAM-CGACTCGTCAGTGCAGGATCAGTGGA-TAMRA

(SEQ ID NO: 13) where FAM (PE-Applied Biosystems, Foster City, Calif.) is the fluorescent reporter dye) and TAMRA (PE-Applied Biosystems, Foster City, Calif.) is the quencher dye. For rat GAPDH the PCR primers were:

forward primer: TGTTCTAGAGACAGCCGCATCTT (SEQ ID NO: 14)

reverse primer: CACCGACCTTCACCATCTTGT (SEQ ID NO: 15) and the PCR probe was: 5'JOE-TTGTGCAGTGCCAGCCTCGTCTCA-TAMRA 3' (SEQ ID NO: 16) where JOE (PE-Applied Biosystems, Foster City, Calif.) is the fluorescent reporter dye) and TAMRA (PE-Applied Biosystems, Foster City, Calif.) is the quencher dye.

Example 14

Northern Blot Analysis of PTP1B mRNA Levels

Eighteen hours after antisense treatment, cell monolayers were washed twice with cold PBS and lysed in 1 mL RNAZOL.TM. reagent (TEL-TEST "B" Inc., Friendswood, Tex.). Total RNA was prepared following manufacturer's recommended protocols. Twenty micrograms of total RNA was fractionated by electrophoresis through 1.2% agarose gels containing 1.1% formaldehyde using a MOPS buffer system (AMRESCO, Inc. Solon, Ohio). RNA was transferred from the gel to HYBOND.TM.-N+ nylon membranes (Amersham Pharmacia Biotech, Piscataway, N.J.) by overnight capillary transfer using a Northern/Southern Transfer buffer system (TEL-TEST "B" Inc., Friendswood, Tex.). RNA transfer was confirmed by UV visualization. Membranes were fixed by UV cross-linking using a STRATALINKER.TM. UV Crosslinker 2400 instrument (Stratagene, Inc, La Jolla, Calif.) and then robed using QUICKHYB.TM. hybridization solution (Stratagene, La Jolla, Calif.) using manufacturer's recommendations for stringent conditions.

To detect human PTP1B, a human PTP1B specific probe was prepared by PCR using the forward primer GGAGTTCGAGCAGATCGACAA (SEQ ID NO: 4) and the reverse primer GGCCACTCTACATGGGAAGTC (SEQ ID NO: 5). To normalize for variations in loading and transfer efficiency membranes were stripped and probed for human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) RNA (Clontech, Palo Alto, Calif.).

To detect rat PTP1B, a rat PTP1B specific probe was prepared by PCR using the forward primer CGAGGGTGCAAAGTTCATCAT (SEQ ID NO:11) and the reverse primer CCAGGTCTTCATGGGAAAGCT (SEQ ID NO: 12). To normalize for variations in loading and transfer efficiency membranes were stripped and probed for rat glyceraldehyde-3-phosphate dehydrogenase (GAPDH) RNA (Clontech, Palo Alto, Calif.).

Hybridized membranes were visualized and quantitated using a PHOSPHORIMAGER.TM. instrument and IMAGEQUANT.TM. Software V3.3 (Molecular Dynamics, Sunnyvale, Calif.). Data was normalized to GAPDH levels in untreated controls.

Example 15

Antisense Inhibition of Human PTP1B Expression by Chimeric Phosphorothioate Oligonucleotides Having 2'-MOE Wings and a Deoxy Gap

In accordance with the present invention, a series of oligonucleotides were designed to target different regions of the human PTP1B RNA, using published sequences (GenBank accession number M31724, incorporated herein as SEQ ID NO: 3). The oligonucleotides are shown in Table 1. "Target site" indicates the first (5'-most) nucleotide number on the particular target sequence to which the oligonucleotide binds. All compounds in Table 1 are chimeric oligonucleotides ("gapmers") 20 nucleotides in length, composed of a central "gap" region consisting of ten 2'-deoxynucleotides, which is flanked on both sides (5' and 3' directions) by five-nucleotide "wings". The wings are composed of 2'-methoxyethyl (T-MOE) nucleotides. The internucleoside (backbone) linkages are phosphorothioate (P.dbd.S) throughout the oligonucleotide. All cytidine residues are 5-methylcytidines. The compounds were analyzed for their effect on human PTP1B mRNA levels by quantitative real-time PCR as described in other examples herein. Data are averages from two experiments. If present, "N.D." indicates "no data".

TABLE-US-00001 TABLE 1 Inhibition of human PTP1B mRNA levels by chimeric phosphorothioate oligonucleotides having 2'-MOE wings and a deoxy gap TARGET SEQ ID TARGET % SEQ ID ISIS # REGION NO SITE SEQUENCE INHIB NO 107769 5' UTR 3 1 cttagccccgaggcccgccc 0 17 107770 5' UTR 3 41 ctcggcccactgcgccgtct 58 18 107771 Start 3 74 catgacgggccagggcggct 60 19 Codon 107772 Coding 3 113 cccggacttgtcgatctgct 95 20 107773 Coding 3 154 ctggcttcatgtcggatatc 88 21 107774 Coding 3 178 ttggccactctacatgggaa 77 22 107775 Coding 3 223 ggactgacgtctctgtacct 75 23 107776 Coding 3 252 gatgtagtttaatccgacta 82 24 107777 Coding 3 280 ctagcgttgatatagtcatt 29 25 107778 Coding 3 324 gggtaagaatgtaactcctt 86 26 107779 Coding 3 352 tgaccgcatgtgttaggcaa 75 27 107780 Coding 3 381 ttttctgctcccacaccatc 30 28 107781 Coding 3 408 ctctgttgagcatgacgaca 78 29 107782 Coding 3 436 gcgcattttaacgaaccttt 83 30 107783 Coding 3 490 aaatttgtgtcttcaaagat 0 31 107784 Coding 3 519 tgatatcttcagagatcaat 57 32 107785 Coding 3 547 tctagctgtcgcactgtata 74 33 107786 Coding 3 575 agtttcttgggttgtaaggt 33 34 107787 Coding 3 604 gtggtatagtggaaatgtaa 51 35 107788 Coding 3 632 tgattcagggactccaaagt 55 36 107789 Coding 3 661 ttgaaaagaaagttcaagaa 17 37 107790 Coding 3 688 gggctgagtgaccctgactc 61 38 107791 Coding 3 716 gcagtgcaccacaacgggcc 81 39 107792 Coding 3 744 aggttccagacctgccgatg 81 40 107793 Coding 3 772 agcaggaggcaggtatcagc 2 41 107794 Coding 3 799 gaagaagggtctttcctctt 53 42 107795 Coding 3 826 tctaacagcactttcttgat 18 43 107796 Coding 3 853 atcaaccccatccgaaactt 0 44 107797 Coding 3 880 gagaagcgcagctggtcggc 82 45 107798 Coding 3 908 tttggcaccttcgatcacag 62 46 107799 Coding 3 952 agctccttccactgatcctg 70 47 107800 Coding 3 1024 tccaggattcgtttgggtgg 72 48 107801 Coding 3 1052 gaactccctgcatttcccat 68 49 107802 Coding 3 1079 ttccttcacccactggtgat 40 50 107803 Coding 3 1148 gtagggtgcggcatttaagg 0 51 107804 Coding 3 1176 cagtgtcttgactcatgctt 75 52 107805 Coding 3 1222 gcctgggcacctcgaagact 67 53 107806 Coding 3 1268 ctcgtccttctcgggcagtg 37 54 107807 Coding 3 1295 gggcttccagtaactcagtg 73 55 107808 Coding 3 1323 ccgtagccacgcacatgttg 80 56 107809 Coding 3 1351 tagcagaggtaagcgccggc 72 57 107810 Stop 3 1379 ctatgtgttgctgttgaaca 85 58 Codon 107811 3' UTR 3 1404 ggaggtggagtggaggaggg 51 59 107812 3' UTR 3 1433 ggctctgcgggcagaggcgg 81 60 107813 3' UTR 3 1460 ccgcggcatgcctgctagtc 84 61 107814 3' UTR 3 1489 tctctacgcggtccggcggc 84 62 107815 3' UTR 3 1533 aagatgggttttagtgcaga 65 63 107816 3' UTR 3 1634 gtactctctttcactctcct 69 64 107817 3' UTR 3 1662 ggccccttccctctgcgccg 59 65 107818 3' UTR 3 1707 ctccaggagggagccctggg 57 66 107819 3' UTR 3 1735 gggctgttggcgtgcgccgc 54 67 107820 3' UTR 3 1783 tttaaataaatatggagtgg 0 68 107821 3' UTR 3 1831 gttcaagaaaatgctagtgc 69 69 107822 3' UTR 3 1884 ttgataaagcccttgatgca 74 70 107823 3' UTR 3 1936 atggcaaagccttccattcc 26 71 107824 3' UTR 3 1973 gtcctccttcccagtactgg 60 72 107825 3' UTR 3 2011 ttacccacaatatcactaaa 39 73 107826 3' UTR 3 2045 attatatattatagcattgt 24 74 107827 3' UTR 3 2080 tcacatcatgtttcttatta 48 75 107828 3' UTR 3 2115 ataacagggaggagaataag 0 76 107829 3' UTR 3 2170 ttacatgcattctaatacac 21 77 107830 3' UTR 3 2223 gatcaaagtttctcatttca 81 78 107831 3' UTR 3 2274 ggtcatgcacaggcaggttg 82 79 107832 3' UTR 3 2309 caacaggcttaggaaccaca 65 80 107833 3' UTR 3 2344 aactgcaccctattgctgag 61 81 107834 3' UTR 3 2380 gtcatgccaggaattagcaa 0 82 107835 3' UTR 3 2413 acaggctgggcctcaccagg 58 83 107836 3' UTR 3 2443 tgagttacagcaagaccctg 44 84 107837 3' UTR 3 2473 gaatatggcttcccataccc 0 85 107838 3' UTR 3 2502 ccctaaatcatgtccagagc 87 86 107839 3' UTR 3 2558 gacttggaatggcggaggct 74 87 107840 3' UTR 3 2587 caaatcacggtctgctcaag 31 88 107841 3' UTR 3 2618 gaagtgtggtttccagcagg 56 89 107842 3' UTR 3 2648 cctaaaggaccgtcacccag 42 90 107843 3' UTR 3 2678 gtgaaccgggacagagacgg 25 91 107844 3' UTR 3 2724 gccccacagggtttgagggt 53 92 107845 3' UTR 3 2755 cctttgcaggaagagtcgtg 75 93 107846 3' UTR 3 2785 aaagccacttaatgtggagg 79 94 107847 3' UTR 3 2844 gtgaaaatgctggcaagaga 86 95 107848 3' UTR 3 2970 tcagaatgcttacagcctgg 61 96

As shown in Table 1, SEQ ID NOs 18, 19, 20, 21, 22, 23, 24, 26, 27, 29, 30, 32, 33, 35, 36, 38, 39, 40, 42, 45, 46, 47, 48, 49, 50, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 69, 70, 72, 73, 75, 78, 79, 80, 81, 83, 84, 86, 87, 89, 90, 92, 93, 94, 95, and 96 demonstrated at least 35% inhibition of human PTP1B expression in this assay and are therefore preferred.

Example 16

Antisense Inhibition of Rat PTP1B Expression by Chimeric Phosphorothioate Oligonucleotides Having 2'-MOE Wings and a Deoxy Gap

In accordance with the present invention, a second series of oligonucleotides were designed to target different regions of the rat PTP1B RNA, using published sequences (GenBank accession number M33962, incorporated herein as SEQ ID NO: 10). The oligonucleotides are shown in Table 2. "Target site" indicates the first (5'-most) nucleotide number on the particular target sequence to which the oligonucleotide binds. All compounds in Table 2 are chimeric oligonucleotides ("gapmers") 20 nucleotides in length, composed of a central "gap" region consisting of ten 2'-deoxynucleotides, which is flanked on both sides (5' and 3' directions) by five-nucleotide "wings". The wings are composed of 2'-methoxyethyl (2'-MOE) nucleotides. The internucleoside (backbone) linkages are phosphoro-thioate (P.dbd.S) throughout the oligonucleotide. All cytidine residues are 5-methylcytidines. The compounds were analyzed for their effect on rat PTP1B mRNA levels by quantitative real-time PCR as described in other examples herein. Data are averages from two experiments. If present, "N.D." indicates "no data".

TABLE-US-00002 TABLE 2 Inhibition of rat PTP1B mRNA levels by chimeric phosphorothioate oligonucleotides having 2'-MOE wings and a deoxy gap TARGET SEQ ID TARGET % SEQ ID ISIS # REGION NO SITE SEQUENCE INHIB NO 111549 5' UTR 10 1 caacctccccagcagcggct 32 97 111550 5' UTR 10 33 tcgaggcccgtcgcccgcca 27 98 111551 5' UTR 10 73 cctcggccgtccgccgcgct 34 99 111552 Coding 10 132 tcgatctgctcgaattcctt 49 100 113669 Coding 10 164 cctggtaaatagccgcccag 36 101 113670 Coding 10 174 tgtcgaatatcctggtaaat 63 102 113671 Coding 10 184 actggcttcatgtcgaatat 58 103 113672 Coding 10 189 aagtcactggcttcatgtcg 40 104 111553 Coding 10 190 gaagtcactggcttcatgtc 27 105 113673 Coding 10 191 ggaagtcactggcttcatgt 54 106 113674 Coding 10 192 gggaagtcactggcttcatg 41 107 113675 Coding 10 193 tgggaagtcactggcttcat 56 108 113676 Coding 10 194 atgggaagtcactggcttca 31 109 113677 Coding 10 195 catgggaagtcactggcttc 59 110 113678 Coding 10 225 tttttgttcttaggaagttt 24 111 111554 Coding 10 228 cggtttttgttcttaggaag 45 112 111555 Coding 10 269 tccgactgtggtcaaaaggg 39 113 113679 Coding 10 273 ttaatccgactgtggtcaaa 45 114 113680 Coding 10 298 atagtcattatcttcctgat 49 115 111556 Coding 10 303 ttgatatagtcattatcttc 29 116 113681 Coding 10 330 gcttcctccatttttatcaa 67 117 111557 Coding 10 359 ggccctgggtgaggatatag 20 118 113682 Coding 10 399 cacaccatctcccagaagtg 29 119 111558 Coding 10 405 tgctcccacaccatctccca 48 120 113683 Coding 10 406 ctgctcccacaccatctccc 51 121 113684 Coding 10 407 tctgctcccacaccatctcc 37 122 113685 Coding 10 408 ttctgctcccacaccatctc 54 123 113686 Coding 10 417 cccctgctcttctgctccca 60 124 111559 Coding 10 438 atgcggttgagcatgaccac 15 125 113687 Coding 10 459 tttaacgagcctttctccat 33 126 113688 Coding 10 492 ttttcttctttctgtggcca 54 127 113689 Coding 10 502 gaccatctctttttcttctt 58 128 111560 Coding 10 540 tcagagatcagtgtcagctt 21 129 113690 Coding 10 550 cttgacatcttcagagatca 64 130 113691 Coding 10 558 taatatgacttgacatcttc 46 131 111561 Coding 10 579 aactccaactgccgtactgt 14 132 111562 Coding 10 611 tctctcgagcctcctgggta 38 133 113692 Coding 10 648 ccaaagtcaggccaggtggt 63 134 111563 Coding 10 654 gggactccaaagtcaggcca 31 135 113693 Coding 10 655 agggactccaaagtcaggcc 50 136 113694 Coding 10 656 cagggactccaaagtcaggc 45 137 113695 Coding 10 657 tcagggactccaaagtcagg 49 138 113696 Coding 10 663 ggtgactcagggactccaaa 34 139 111564 Coding 10 705 cctgactctcggactttgaa 53 140 113697 Coding 10 715 gctgagtgagcctgactctc 57 141 113698 Coding 10 726 ccgtgctctgggctgagtga 48 142 111565 Coding 10 774 aaggtccctgacctgccaat 28 143 111566 Coding 10 819 tctttcctcttgtccatcag 34 144 113699 Coding 10 820 gtctttcctcttgtccatca 41 145 113700 Coding 10 821 ggtctttcctcttgtccatc 66 146 113701 Coding 10 822 gggtctttcctcttgtccat 71 147 113702 Coding 10 852 aacagcactttcttgatgtc 39 148 111567 Coding 10 869 ggaacctgcgcatctccaac 0 149 111568 Coding 10 897 tggtcggccgtctggatgag 29 150 113703 Coding 10 909 gagaagcgcagttggtcggc 48 151 113704 Coding 10 915 aggtaggagaagcgcagttg 31 152 113705 Coding 10 918 gccaggtaggagaagcgcag 41 153 111569 Coding 10 919 agccaggtaggagaagcgca 56 154 113706 Coding 10 920 cagccaggtaggagaagcgc 58 155 113707 Coding 10 921 acagccaggtaggagaagcg 43 156 113708 Coding 10 922 cacagccaggtaggagaagc 49 157 113709 Coding 10 923 tcacagccaggtaggagaag 47 158 111570 Coding 10 924 atcacagccaggtaggagaa 51 159 113710 Coding 10 925 gatcacagccaggtaggaga 51 160 113711 Coding 10 926 cgatcacagccaggtaggag 63 161 113712 Coding 10 927 tcgatcacagccaggtagga 71 162 113713 Coding 10 932 caccctcgatcacagccagg 75 163 113714 Coding 10 978 tccttccactgatcctgcac 97 164 111571 Coding 10 979 ctccttccactgatcctgca 89 165 113715 Coding 10 980 gctccttccactgatcctgc 99 166 107799 Coding 10 981 agctccttccactgatcctg 99 167 113716 Coding 10 982 aagctccttccactgatcct 97 168 113717 Coding 10 983 aaagctccttccactgatcc 95 169 113718 Coding 10 984 gaaagctccttccactgatc 95 170 113719 Coding 10 985 ggaaagctccttccactgat 95 171 111572 Coding 10 986 gggaaagctccttccactga 89 172 113720 Coding 10 987 tgggaaagctccttccactg 97 173 113721 Coding 10 1036 tggccggggaggtgggggca 20 174 111573 Coding 10 1040 tgggtggccggggaggtggg 20 175 113722 Coding 10 1046 tgcgtttgggtggccgggga 18 176 111574 Coding 10 1073 tgcacttgccattgtgaggc 38 177 113723 Coding 10 1206 acttcagtgtcttgactcat 67 178 113724 Coding 10 1207 aacttcagtgtcttgactca 60 179 111575 Coding 10 1208 taacttcagtgtcttgactc 50 180 113725 Coding 10 1209 ctaacttcagtgtcttgact 53 181 111576 Coding 10 1255 gacagatgcctgagcacttt 32 182 106409 Coding 10 1333 gaccaggaagggcttccagt 32 183 113726 Coding 10 1334 tgaccaggaagggcttccag 39 184 111577 Coding 10 1335 ttgaccaggaagggcttcca 32 185 113727 Coding 10 1336 gttgaccaggaagggcttcc 41 186 113728 Coding 10 1342 gcacacgttgaccaggaagg 59 187 111578 Coding 10 1375 gaggtacgcgccagtcgcca 45 188 111579 Coding 10 1387 tacccggtaacagaggtacg 32 189 111580 Coding 10 1397 agtgaaaacatacccggtaa 30 190 111581 3' UTR 10 1456 caaatcctaacctgggcagt 31 191 111582 3' UTR 10 1519 ttccagttccaccacaggct 24 192 111583 3' UTR 10 1552 ccagtgcacagatgcccctc 47 193 111584 3' UTR 10 1609 acaggttaaggccctgagat 29 194 111585 3' UTR 10 1783 gcctagcatcttttgttttc 43 195 111586 3' UTR 10 1890 aagccagcaggaactttaca 36 196 111587 3' UTR 10 2002 gggacacctgagggaagcag 16 197 111588 3' UTR 10 2048 ggtcatctgcaagatggcgg 40 198 111589 3' UTR 10 2118 gccaacctctgatgaccctg 25 199 111590 3' UTR 10 2143 tggaagccccagctctaagc 25 200 111591 3' UTR 10 2165 tagtaatgactttccaatca 44 201 111592 3' UTR 10 2208 tgagtcttgctttacacctc 41 202 111593 3' UTR 10 2252 cctgcgcgcggagtgacttc 22 203 111594 3' UTR 10 2299 aggacgtcactgcagcagga 43 204 111595 3' UTR 10 2346 tcaggacaagtcttggcagt 32 205 111596 3' UTR 10 2405 gaggctgcacagtaagcgct 34 206 111597 3' UTR 10 2422 tcagccaaccagcatcagag 20 207 111598 3' UTR 10 2449 acccacagtgtccacctccc 30 208 111599 3' UTR 10 2502 agtgcgggctgtgctgctgg 30 209 111600 3' UTR 10 2553 cagctcgctctggcggcctc 8 210 111601 3' UTR 10 2608 aggaagggagctgcacgtcc 32 211 111602 3' UTR 10 2664 ccctcacgattgctcgtggg 24 212 111603 3' UTR 10 2756 cagtggagcggctcctctgg 18 213 111604 3' UTR 10 2830 caggctgacaccttacacgg 30 214 111605 3' UTR 10 2883 gtcctacctcaaccctagga 37 215 111606 3' UTR 10 2917 ctgccccagcaccagccaca 12 216 111607 3' UTR 10 2946 attgcttctaagaccctcag 33 217

111608 3' UTR 10 2978 ttacatgtcaccactgttgt 28 218 111609 3' UTR 10 3007 tacacatgtcatcagtagcc 37 219 111610 3' UTR 10 3080 ttttctaactcacagggaaa 30 220 111611 3' UTR 10 3153 gtgcccgccagtgagcaggc 23 221 111612 3' UTR 10 3206 cggcctcggcactggacagc 27 222 111613 3' UTR 10 3277 gtggaatgtctgagatccag 31 223 111614 3' UTR 10 3322 agggcgggcctgcttgccca 23 224 111615 3' UTR 10 3384 cggtcctggcctgctccaga 31 225 111616 3' UTR 10 3428 tacactgttcccaggagggt 42 226 111617 3' UTR 10 3471 tggtgccagcagcgctagca 10 227 111618 3' UTR 10 3516 cagtctcttcagcctcaaga 43 228 113729 3' UTR 10 3537 aagagtcatgagcaccatca 56 229 111619 3' UTR 10 3560 tgaaggtcaagttcccctca 40 230 111620 3' UTR 10 3622 ctggcaagaggcagactgga 30 231 111621 3' UTR 10 3666 ggctctgtgctggcttctct 52 232 111622 3' UTR 10 3711 gccatctcctcagcctgtgc 39 233 111623 3' UTR 10 3787 agcgcctgctctgaggcccc 16 234 111624 3' UTR 10 3854 tgctgagtaagtattgactt 35 235 111625 3' UTR 10 3927 ctatggccatttagagagag 36 236 113730 3' UTR 10 3936 tggtttattctatggccatt 59 237 111626 3' UTR 10 3994 cgctcctgcaaaggtgctat 11 238 111627 3' UTR 10 4053 gttggaaacggtgcagtcgg 39 239 111628 3' UTR 10 4095 atttattgttgcaactaatg 33 240

As shown in Table 2, SEQ ID NOs 97, 99, 100, 101, 102, 103, 104, 106, 107, 108, 109, 110, 112, 113, 114, 115, 117, 120, 121, 122, 123, 124, 126, 127, 128, 130, 131, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 144, 145, 146, 147, 148, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 191, 193, 195, 196, 198, 201, 202, 204, 205, 206, 211, 215, 217, 219, 223, 225, 226, 228, 229, 230, 232, 233, 235, 236, 237, 239 and 240 demonstrated at least 30% inhibition of rat PTP1B expression in this experiment and are therefore preferred.

Example 17

Western Blot Analysis of PTP1B Protein Levels

Western blot analysis (immunoblot analysis) is carried out using standard methods. Cells are harvested 16-20 h after oligonucleotide treatment, washed once with PBS, suspended in Laemmli buffer (100 .mu.L/well), boiled for 5 minutes and loaded on a 16% SDS-PAGE gel. Gels are run for 1.5 hours at 150 V, and transferred to membrane for western blotting. Appropriate primary antibody directed to PTP1B is used, with a radiolabelled or fluorescently labeled secondary antibody directed against the primary antibody species. Bands are visualized using a PHOSPHORIMAGER.TM. instrument (Molecular Dynamics, Sunnyvale Calif.).

Example 18

Effects of Antisense Inhibition of PTP1B (ISIS 113715) on Blood Glucose Levels

db/db mice are used as a model of Type 2 diabetes. These mice are hyperglycemic, obese, hyperlipidemic, and insulin resistant. The db/db phenotype is due to a mutation in the leptin receptor on a C57BLKS background. However, a mutation in the leptin gene on a different mouse background can produce obesity without diabetes (ob/ob mice). Leptin is a hormone produced by fat that regulates appetite and animals or humans with leptin deficiencies become obese. Heterozygous db/wt mice (known as lean littermates) do not display the hyperglycemia/hyperlipidemia or obesity phenotype and are used as controls.

In accordance with the present invention, ISIS 113715 (GCTCCTTCCACTGATCCTGC, SEQ ID No: 166) was investigated in experiments designed to address the role of PTP1B in glucose metabolism and homeostasis. ISIS 113715 is completely complementary to sequences in the coding region of the human, rat, and mouse PTP1B nucleotide sequences incorporated herein as SEQ ID No: 3 (starting at nucleotide 951 of human PTP1B; Genbank Accession No. M31724), SEQ ID No: (starting at nucleotide 980 of rat PTP1B; Genbank Accession No. M33962) and SEQ ID No: 241 (starting at nucleotide 1570 of mouse PTP1B; Genbank Accession No. U24700). The control used is ISIS 29848 (NNNNNNNNNNNNNNNNNNNN, SEQ ID No: 242) where N is a mixture of A, G, T and C.

Male db/db mice and lean (heterozygous, i.e., db/wt) littermates (age 9 weeks at time 0) were divided into matched groups (n=6) with the same average blood glucose levels and treated by intraperitoneal injection once a week with saline, ISIS 29848 (the control oligonucleotide) or ISIS 113715. db/db mice were treated at a dose of 10, 25 or 50 mg/kg of ISIS 113715 or 50 mg/kg of ISIS 29848 while lean littermates were treated at a dose of 50 or 100 mg/kg of ISIS 113715 or 100 mg/kg of ISIS 29848. Treatment was continued for 4 weeks with blood glucose levels being measured on day 0, 7, 14, 21 and 28.

By day 28 in db/db mice, blood glucose levels were reduced at all doses from a starting level of 300 mg/dL to 225 mg/dL for the 10 mg/kg dose, 175 mg/dL for the 25 mg/kg dose and 125 mg/dL for the 50 mg/kg dose. These final levels are within normal range for wild-type mice (170 mg/dL). The mismatch control and saline treated levels were 320 mg/dL and 370 mg/dL at day 28, respectively.

In lean littermates, blood glucose levels remained constant throughout the study for all treatment groups (average 120 mg/dL). These results indicate that treatment with ISIS 113715 reduces blood glucose in db/db mice and that there is no hypoglycemia induced in the db/db or the lean littermate mice as a result of the oligonucleotide treatment.

In a similar experiment, ob/ob mice and their lean littermates (heterozygous, i.e., ob/wt) were dosed twice a week at 50 mg/kg with ISIS 113715, ISIS 29848 or saline control and blood glucose levels were measured at the end of day 7, 14 and 21. Treatment of ob/ob mice with ISIS 113715 resulted in the largest decrease in blood glucose over time going from 225 mg/dL at day 7 to 95 mg/dL at day 21. Ob/ob mice displayed an increase in plasma glucose over time from 300 mg/dL to 325 mg/dL while treatment with the control oligonucleotide reduced plasma glucose from an average of 280 mg/dL to 130 mg/dL. In the lean littermates plasma glucose levels remained unchanged in all treatment groups (average level 100 mg/dL).

Example 19

Effects of Antisense Inhibition of PTP1B (ISIS 113715) on mRNA Expression in Liver

Male db/db mice and lean littermates (age 9 weeks at time 0) were divided into matched groups (n=6) with the same average blood glucose levels and treated by intraperitoneal injection once a week with saline, ISIS 29848 (the control oligonucleotide) or ISIS 113715. db/db mice were treated at a dose of 10, 25 or 50 mg/kg of ISIS 113715 or 50 mg/kg of ISIS 29848 while lean littermates were treated at a dose of 50 or 100 mg/kg of ISIS 113715 or 100 mg/kg of ISIS 29848. Treatment was continued for 4 weeks after which the mice were sacrificed and tissues collected for mRNA analysis. RNA values were normalized and are expressed as a percentage of saline treated control.

ISIS 113715 successfully reduced PTP1B mRNA levels in the livers of db/db mice at all doses examined (60% reduction of PTP1B mRNA), whereas the control oligonucleotide treated animals showed no reduction in PTP1B mRNA, remaining at the level of the saline treated control. Treatment of lean littermates with ISIS 113715 also reduced mRNA levels to 45% of control at the 50 mg/kg dose and 25% of control at the 100 mg/kg dose. The control oligonucleotide (ISIS 29848) failed to show any reduction in mRNA levels.

Example 20

Effects of Antisense Inhibition of PTP1B (ISIS 113715) on Body Weight

Male db/db mice and lean littermates (age 9 weeks at time 0) were divided into matched groups (n=6) with the same average blood glucose levels and treated by intraperitoneal injection once a week with saline, ISIS 29848 (the control oligonucleotide) or ISIS 113715. db/db mice were treated at a dose of 10, 25 or 50 mg/kg of ISIS 113715 or 50 mg/kg of ISIS 29848 while lean littermates were treated at a dose of 50 or 100 mg/kg of ISIS 113715 or 100 mg/kg of ISIS 29848. Treatment was continued for 4 weeks. At day 28 mice were sacrificed and final body weights were measured.

Treatment of ob/ob mice with ISIS 113715 resulted in an increase in body weight which was constant over the dose range with animals gaining an average of 11.0 grams while saline treated controls gained 5.5 grams. Animals treated with the control oligonucleotide gained an average of 7.8 grams of body weight.

Lean littermate animals treated with 50 or 100 mg/kg of ISIS 113715 gained 3.8 grams of body weight compared to a gain of 3.0 grams for the saline controls.

In a similar experiment, ob/ob mice and their lean littermates were dosed twice a week at 50 mg/kg with ISIS 113715, ISIS 29848 or saline control and body weights were measured at the end of day 7, 14 and 21.

Treatment of the ob/ob mice with ISIS 113715, ISIS 29848 or saline control all resulted in a similar increase in body weight across the 21-day timecourse. At the end of day 7 all ob/ob treatment groups had an average weight of 42 grams. By day 21, animals treated with ISIS 113715 had an average body weight of 48 grams, while those in the ISIS 29848 (control oligonucleotide) and saline control group each had an average body weight of 52 grams. All of the lean littermates had an average body weight of 25 grams at the beginning of the timecourse and all lean littermate treatment groups showed an increase in body weight, to 28 grams, by day 21.

Example 21

Effects of Antisense Inhibition of PTP1B (ISIS 113715) on Plasma Insulin Levels

Male db/db mice (age 9 weeks at time 0) were divided into matched groups (n=6) with the same average blood glucose levels and treated by intraperitoneal injection twice a week with saline, ISIS 29848 (the control oligonucleotide) or ISIS 113715 at a dose of 50 mg/kg. Treatment was continued for 3 weeks with plasma insulin levels being measured on day 7, 14, and 21.

Mice treated with ISIS 113715 showed a decrease in plasma insulin levels from 15 ng/mL at day 7 to 7.5 ng/mL on day 21. Saline treated animals have plasma insulin levels of 37 ng/mL at day 7, which dropped to 25 ng/mL on day 14, but rose again to 33 ng/mL by day 21. Mice treated with the control oligonucleotide also showed a decrease in plasma insulin levels across the timecourse of the study from 25 ng/mL at day 7 to 10 ng/mL on day 21. However, ISIS 113715 was the most effective at reducing plasma insulin over time.

Example 22

Antisense Inhibition of Human PTP1B Expression by Additional Chimeric Phosphorothioate Oligonucleotides Having 2'-MOE Wings and a Deoxy Gap

In accordance with the present invention, an additional series of oligonucleotides were designed to target different genomic regions of the human PTP1B RNA, using published sequences (GenBank accession number M31724, incorporated herein as SEQ ID NO: 3), and concatenated genomic sequence derived from nucleotide residues 1-31000 of Genbank accession number AL034429 followed by nucleotide residues 1-45000 of Genbank accession number AL133230, incorporated herein as SEQ ID NO: 243). The oligonucleotides are shown in Table 3. "Target site" indicates the first (5'-most) nucleotide number on the particular target sequence to which the oligonucleotide binds. All compounds in Table 3 are chimeric oligonucleotides ("gapmers") 20 nucleotides in length, composed of a central "gap" region consisting of ten 2'-deoxynucleotides, which is flanked on both sides (5' and 3' directions) by five-nucleotide "wings". The wings are composed of 2'-methoxyethyl (2'-MOE) nucleotides. The internucleoside (backbone) linkages are phosphoro-thioate (P.dbd.S) throughout the oligonucleotide. All cytidine residues are 5-methylcytidines. The compounds were analyzed for their effect on human PTP1B mRNA levels by quantitative real-time PCR as described in other examples herein. Data are averages from two experiments. If present, "N.D." indicates "no data".

TABLE-US-00003 TABLE 3 Inhibition of human PTP1B mRNA levels by chimeric phosphorothioate oligonucleotides having 2'-MOE wings and a deoxy gap TARGET SEQ ID TARGET % SEQ ID Isis # REGION NO SITE SEQUENCE INHIB NO 142020 5' UTR 3 6 GCGCTCTTAGCCCCGAGGCC 61 244 142021 5' UTR 3 65 CCAGGGCGGCTGCTGCGCCT 56 245 142022 Start Codon 3 80 CATCTCCATGACGGGCCAGG 4 246 142023 Start Codon 3 85 TTTTCCATCTCCATGACGGG 67 247 142024 Start Codon 3 90 ACTCCTTTTCCATCTCCATG 71 248 142025 Exon 1 3 106 TTGTCGATCTGCTCGAACTC 61 249 142026 Exon 1 3 109 GACTTGTCGATCTGCTCGAA 66 250 142027 Exon 1 3 116 GCTCCCGGACTTGTCGATCT 95 251 142028 Exon 1 3 119 CCAGCTCCCGGACTTGTCGA 92 252 142029 Exon:Exon 3 945 TCCACTGATCCTGCACGGAA 44 253 Junction 142030 Exon:Exon 3 948 CCTTCCACTGATCCTGCACG 55 254 Junction 142031 3' UTR 3 1453 ATGCCTGCTAGTCGGGCGTG 67 255 142032 3' UTR 3 1670 CGGGTGTAGGCCCCTTCCCT 74 256 142033 3' UTR 3 1772 ATGGAGTGGAGAGTTGCTCC 63 257 142034 3' UTR 3 1893 TTGTACTTTTTGATAAAGCC 61 258 142035 3' UTR 3 1962 CAGTACTGGTCTGACGCAGC 68 259 142036 3' UTR 3 2018 TCTCACGTTACCCACAATAT 74 260 142037 3' UTR 3 2070 TTTCTTATTAAATACCCACG 61 261 142038 3' UTR 3 2088 AAGTAATCTCACATCATGTT 79 262 142039 3' UTR 3 2314 TTCAGCAACAGGCTTAGGAA 51 263 142040 3' UTR 3 2323 GACAATGACTTCAGCAACAG 43 264 142041 3' UTR 3 2359 TGCCTATTCCTGGAAAACTG 43 265 142042 3' UTR 3 2395 GGAAGTCACTAGAGTGTCAT 14 266 142043 3' UTR 3 2418 CCAGGACAGGCTGGGCCTCA 67 267 142044 3' UTR 3 2426 CTGCTGTACCAGGACAGGCT 73 268 142045 3' UTR 3 2452 TGGAATGTCTGAGTTACAGC 74 269 142046 3' UTR 3 2566 AGAGTGTTGACTTGGAATGG 43 270 142047 3' UTR 3 2574 GCTCAAGAAGAGTGTTGACT 76 271 142048 3' UTR 3 2598 TGCCTCTCTTCCAAATCACG 43 272 142049 3' UTR 3 2800 TGTTTTTCATGTTAAAAAGC 44 273 142050 3' UTR 3 2895 TCCCACCACAGAATTTCTCT 21 274 142051 3' UTR 3 2921 GCTCTGCAGGGTGACACCTC 74 275 142052 3' UTR 3 3066 AGGAGGTTAAACCAGTACGT 78 276 142053 3' UTR 3 3094 GGTGGAGAGCCAGCTGCTCT 59 277 142054 3' UTR 3 3153 TATTGGCTTAAGGCATATAG 72 278 142055 3' UTR 3 3168 GACCTGATGAGTAAATATTG 58 279 142084 5' UTR 243 859 TTCTTCATGTCAACCGGCAG 11 280 142085 5' UTR 243 919 GCCCCGAGGCCCGCTGCAAT 83 281 142056 Intron 1 243 4206 TAGTGAACTATTGTTACAAC 70 282 142057 Intron 1 243 27032 TGCTAAGCCACTTCTAATCA 72 283 142058 Intron 1 243 27203 CAGGATTCTAAGTTATTAAA 32 284 142059 Intron 1 243 33720 TGGGCAGGATGGCTCTGGTA 21 285 142060 Intron 1 243 48065 TACAATACTATCTGTGACTA 34 286 142061 Exon: 243 51931 GATACTTACAGGGACTGACG 39 287 Intron Junction 142086 Intron 2 243 52005 AACCCTGAGGCGAAAGGAG 64 288 142062 Intron 2 243 54384 CCCCAGGTCACTAAAATTAA 48 289 142063 Intron 2 243 55362 AAAGCAAAGGTGAGTTGGT 56 290 142064 Intron 3 243 56093 GCTCAATTATTAAACCACTT 64 291 142065 Intron 3 243 56717 AGTCCTCAAGAAGTCACTTT 70 292 142066 Intron 4 243 61780 GAAAGCAGGGACTGCTGGC 39 293 142067 Intron 4 243 64554 AAAACTGGGAGAGACAGCA 71 294 142068 Intron 4 243 64869 ACATGGAAGCCATGGTCAGC 24 295 142069 Intron 5 243 67516 ATTGCTAGACTCACACTAGG 68 296 142070 Intron 5 243 68052 GGCTGTGATCAAAAGGCAG 51 297 142087 Intron 5 243 68481 CACTGGCTCTGGGCAACTTT 70 298 142088 Intron 5 243 68563 GCTGGGCAGCCACCCATAAA 71 299 142071 Intron 5 243 68648 AGTCCCCTCACCTCTTTTCT 59 300 142072 Exon: 243 69107 CCTCCTTACCAGCAAGAGGC 26 301 Intron 142089 Intron 6 243 69198 TGTATTTTGGAAGAGGAGCG 53 302 142090 Intron 6 243 69220 ACAGACTAACACAGTGAGTC 53 303 142073 Intron 6 243 69264 ACAAATTACCGAGTCTCAGG 47 304 142074 Intron 6 243 69472 TCATGAAAGGCTTGGTGCCC 41 305 142075 Intron 7 243 70042 TTGGAAGATGAAATCTTTTG 30 306 142076 Intron 7 243 70052 AGCCATGTACTTGGAAGATG 69 307 142077 Intron 8 243 70661 CGAGCCCCTCATTCCAACAA 42 308 142078 Intron 8 243 71005 CACCTCAGCGGACACCTCTA 6 309 142079 Exon: 243 71938 GAAACATACCCTGTAGCAGA 52 310 Intron 142091 Intron 9 243 72131 CAGAGGGCTCCTTAAAACCC 61 311 142092 Intron 9 243 72430 ATTCGTAAAAGTTTGGGATT 34 312 142080 Intron 9 243 72453 CCCTCTTCTCCAAGGGAGTT 73 313 142081 Intron 9 243 73158 GGAATGAAACCAAACAGTT 42 314 142082 Exon 10 243 75012 AAATGGTTTATTCCATGGCC 66 315 142083 Exon 10 243 75215 AAAAATTTTATTGTTGCAGC 48 316 142093 3' UTR 243 75095 CCGGTCATGCAGCCACGTAT 85 317 142094 3' UTR 243 75165 GTTGGAAAACTGTACAGTCT 77 318 142095 3' UTR 243 75211 ATTTTATTGTTGCAGCTAAA 46 319

As shown in Table 3, SEQ ID NOs, 244, 245, 247, 248, 249, 250, 251, 252, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 267, 268, 269, 271, 275, 276, 277, 278, 279, 281, 282, 283, 288, 290, 291, 292, 294, 296, 297, 298, 299, 300, 302, 303, 307, 310, 311, 313, 315, 317, and 318, demonstrated at least 50% inhibition of human PTP1B expression in this assay and are therefore preferred.

Example 23

Antisense Inhibition of Human PTP1B Expression by Additional Chimeric Phosphorothioate Oligonucleotides Having 2'-MOE Wings and a Deoxy Gap

In accordance with the present invention, an additional series of oligonucleotides were designed to target either the 3'UTR or the 5'UTR of the human PTP1B RNA, using published sequences (GenBank accession number M31724, incorporated herein as SEQ ID NO: 3) and concatenated genomic sequence derived from nucleotide residues 1-31000 of Genbank accession number AL034429 followed by nucleotide residues 1-45000 of Genbank accession number AL133230, incorporated herein as SEQ ID NO: 243. The oligonucleotides are shown in Table 4. "Target site" indicates the first (5'-most) nucleotide number on the particular target sequence to which the oligonucleotide binds. All compounds in Table 3 are chimeric oligonucleotides ("gapmers") 20 nucleotides in length, composed of a central "gap" region consisting of ten 2'-deoxynucleotides, which is flanked on both sides (5' and 3' directions) by five-nucleotide "wings". The wings are composed of 2'-methoxyethyl (2'-MOE) nucleotides. The internucleoside (backbone) linkages are phosphoro-thioate (P.dbd.S) throughout the oligonucleotide. All cytidine residues are 5-methylcytidines. The compounds were analyzed for their effect on human PTP1B mRNA levels by quantitative real-time PCR as described in other examples herein. Data are averages from two experiments. If present, "N.D." indicates "no data".

TABLE-US-00004 TABLE 4 Inhibition of human PTP1B mRNA levels by chimeric phosphorothioate oligonucleotides having 2'-MOE wings and a deoxy gap TARGET SEQ ID TARGET % SEQ ID ISIS # REGION NO. SITE SEQUENCE INHIB NO. 146879 5' UTR 3 50 CGCCTCCTTCTCGGCCCACT 29 320 146880 5' UTR 3 62 GGGCGGCTGCTGCGCCTCCT 34 321 146881 3' UTR 3 1601 GTGGATTTGGTACTCAAAGT 72 322 146882 3' UTR 3 1610 AAATGGCTTGTGGATTTGGT 72 323 146883 3' UTR 3 1637 ATGGTACTCTCTTTCACTCT 61 324 146884 3' UTR 3 1643 GCCAGCATGGTACTCTCTTT 63 325 146885 3' UTR 3 1764 GAGAGTTGCTCCCTGCAGAT 62 326 146886 3' UTR 3 1770 GGAGTGGAGAGTTGCTCCC 57 327 146887 3' UTR 3 1874 CCTTGATGCAAGGCTGACAT 65 328 146888 3' UTR 3 1879 AAAGCCCTTGATGCAAGGC 59 329 146889 3' UTR 3 1915 AGTACTACCTGAGGATTTAT 46 330 146890 3' UTR 3 1925 TTCCATTCCCAGTACTACCT 41 331 146891 3' UTR 3 1938 CCATGGCAAAGCCTTCCATT 65 332 146892 3' UTR 3 1943 CAGGCCCATGGCAAAGCCT 52 333 146893 3' UTR 3 1988 CAACTGCTTACAACCGTCCT 60 334 146894 3' UTR 3 2055 CCACGTGTTCATTATATATT 42 335 146895 3' UTR 3 2063 TTAAATACCCACGTGTTCAT 27 336 146896 3' UTR 3 2099 TAAGCGGGACAAAGTAATC 47 337 146897 3' UTR 3 2118 CAGATAACAGGGAGGAGAA 31 338 146898 3' UTR 3 2133 GAGAACTAGATCTAGCAGA 0 339 146899 3' UTR 3 2140 AGTGATTGAGAACTAGATC 62 340 146900 3' UTR 3 2184 GACACAAGAAGACCTTACA 49 341 146901 3' UTR 3 2212 CTCATTTCAAGCACATATTT 60 342 146902 3' UTR 3 2263 GGCAGGTTGGACTTGGACA 49 343 146903 3' UTR 3 2296 AACCACAGCCATGTAATGA 43 344 146904 3' UTR 3 2332 TTGCTGAGCGACAATGACTT 42 345 146905 3' UTR 3 2350 CTGGAAAACTGCACCCTATT 31 346 146906 3' UTR 3 2409 GCTGGGCCTCACCAGGAAG 77 347 146907 3' UTR 3 2439 TTACAGCAAGACCCTGCTGT 28 348 146908 3' UTR 3 2457 ACCCTTGGAATGTCTGAGTT 65 349 146909 3' UTR 3 2464 TTCCCATACCCTTGGAATGT 62 350 146910 3' UTR 3 2471 ATATGGCTTCCCATACCCTT 47 351 146911 3' UTR 3 2477 GTGTGAATATGGCTTCCCAT 54 352 146912 3' UTR 3 2509 CCTGCTTCCCTAAATCATGT 65 353 146913 3' UTR 3 2514 GTGTCCCTGCTTCCCTAAAT 55 354 146914 3' UTR 3 2546 CGGAGGCTGATCCCAAAGG 55 355 146915 3' UTR 3 2602 CAGGTGCCTCTCTTCCAAAT 60 356 146916 3' UTR 3 2613 GTGGTTTCCAGCAGGTGCCT 63 357 146917 3' UTR 3 2628 GCTGTTTCAAGAAGTGTGGT 43 358 146918 3' UTR 3 2642 GGACCGTCACCCAGGCTGTT 32 359 146919 3' UTR 3 2655 CAGGCTGCCTAAAGGACCG 60 360 146920 3' UTR 3 2732 ACCATCAGGCCCCACAGGG 58 361 146921 3' UTR 3 2759 GTTCCCTTTGCAGGAAGAGT 69 362 146922 3' UTR 3 2772 GTGGAGGTCTTCAGTTCCCT 64 363 146923 3' UTR 3 2781 CCACTTAATGTGGAGGTCTT 54 364 146924 3' UTR 3 2814 AGCTACAGCTGCCGTGTTTT 51 365 146925 3' UTR 3 2862 CCACGAGAAAGGCAAAATG 50 366 146926 3' UTR 3 2885 GAATTTCTCTGTACTGGCTT 23 367 146927 3' UTR 3 2890 CCACAGAATTTCTCTGTACT 61 368 146928 3' UTR 3 2901 GAATGTTCCCACCACAGAA 61 369 146929 3' UTR 3 2956 GCCTGGCACCTAAGCCTTAT 0 370 146930 3' UTR 3 2965 ATGCTTACAGCCTGGCACCT 55 371 146931 3' UTR 3 3008 CTACATACATATACAGGACT 65 372 146932 3' UTR 3 3042 TTTGAAATGCTACTATATAT 44 373 146933 3' UTR 3 3070 GGATAGGAGGTTAAACCAG 67 374 146934 3' UTR 3 3086 GCCAGCTGCTCTCCAAGGAT 42 375 146935 3' UTR 3 3121 CTACCTCTCTAACATAATGT 39 376 146936 3' UTR 3 3126 GCTCGCTACCTCTCTAACAT 68 377 146937 3' UTR 3 3143 AGGCATATAGCAGAGCAGC 61 378 146938 5' UTR 243 851 GTCAACCGGCAGCCGGAAC 14 379 146942 5' UTR 243 891 CCTGCAGCTACCGCCGCCCT 69 380 146943 5' UTR 243 908 CGCTGCAATCCCCGACCCCT 87 381 146944 3' UTR 243 75050 ACCAAAACACCTTGCTTTTT 27 382 146945 3' UTR 243 75057 GTATTATACCAAAACACCTT 39 383 146946 3' UTR 243 75072 CACACACCTGAAAAGGTAT 42 384 146947 3' UTR 243 75097 ACCCGGTCATGCAGCCACG 49 385 146948 3' UTR 243 75136 GTGAGGTCACAGAAGACCC 49 386 146949 3' UTR 243 75154 GTACAGTCTGACAGTTCTGT 40 387 146950 3' UTR 243 75172 ATGGCAAGTTGGAAAACTG 65 388 146951 3' UTR 243 75192 AATGCAAACCCATCATGAA 43 389

As shown in Table 4, SEQ ID NOs, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 337, 340, 341, 342, 343, 344, 345, 347, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 360, 361, 362, 363, 364, 365, 366, 368, 369, 371, 372, 373, 374, 375, 377, 378, 380, 381, 384, 385, 386, 387, 388, and 389 demonstrated at least 40% inhibition of human PTP1B expression in this assay and are therefore preferred.

Example 24

Antisense Inhibition of PTP1B Expression (ISIS 113715) in Liver, Muscle and Adipose Tissue of the Cynomolgus Monkey

In a further embodiment, male cynomolgus monkeys were treated with ISIS 113715 (SEQ ID NO: 166) and levels of PTP1B mRNA and protein were measured in muscle, adipose and liver tissue. Serum samples were also measured for insulin levels.

Male cynomolgus monkeys were divided into two treatment groups, control animals (n=4; saline treatment only) and treated animals (n=8; treated with ISIS 113715). All animals had two pre-dosing glucose tolerance tests (GTTs) performed to establish insulin and glucose baseline values. Animals in the treatment group were dosed subcutaneously on days 1, 8, and 15 with 3 mg/kg, 6 mg/kg and 12 mg/kg of ISIS 113715, respectively. Animals in the control group were untreated. All animals had GTTs performed on days 5, 13 and 19, four days post-dosing. Ten days after the last dose of 12 mg/kg, all animals in the treatment group (ISIS 113715) received a one-time dose of 6 mg/kg of ISIS 113715. Three days later, all animals were sacrificed and tissues were taken for analysis of PTP1B mRNA and protein levels. Levels of mRNA and protein were normalized to those of the saline treated animals. Of the tissue examined, PTP1B mRNA levels were reduced to the greatest extent in the fat and liver, being reduced by 41% and 40%, respectively. mRNA levels in muscle were reduced by 10%. Protein levels were reduced by 60% in the liver and by 45% in the muscle but were shown to increase by 10% in the fat.

Levels of the liver enzymes ALT and AST were measured weekly and showed no change, indicating no ongoing toxic effects of the oligonucleotide treatment.

The results of this study demonstrate a significant reduction in liver PTP1B mRNA and protein upon treatment with ISIS 113715. Furthermore, there was no change seen in the fasting insulin levels either between groups or between pre-treatment and post-treatment of the same group. There was, however, a significant lowering of insulin levels with no decrease in fasting glucose levels in all groups suggesting that insulin efficiency (sensitivity) was increased upon treatment with ISIS 113715.

Example 25

Effects of Antisense Inhibition of PTP1B (ISIS 113715) on mRNA Expression in Fractionated Liver

Male db/db mice (age 9 weeks at time 0) were divided into matched groups (n=6) with the same average blood glucose levels and treated by intraperitoneal injection once a week with saline, ISIS 29848 (the control oligonucleotide) or ISIS 113715. db/db mice were treated at a dose of 50 mg/kg of ISIS 113715 or 50 mg/kg of ISIS 29848 or 100 mg/kg of ISIS 29848. Treatment was continued for 3 weeks after which the mice were sacrificed and tissues were collected for analysis. Liver tissue was removed and homogenized whole or fractionated into hepatocytes and non-parenchymal (NP) cell fractions by standard methods (Graham et al., J. Pharmacol. Exp. Ther., 1998, 286, 447-458). During the study, plasma glucose levels were measured as were PTP1B mRNA levels in both cell fractions. RNA values were normalized and are expressed as a percentage of saline treated control.

Treatment of db/db mice with ISIS 113715 caused a significant reduction in plasma glucose levels (saline=500+/-25 vs. treated=223+/-21 mg/dL; p=0.0001).

ISIS 113715 successfully reduced PTP1B mRNA levels in both hepatocytes and NP cell fractions, with an 80% reduction in hepatocytes and a 30% reduction in the NP cell fraction. In addition, PTP1B expression in the two cell fractions was found to be dramatically different with a 5-8 fold greater level of expression being found in the NP fraction. Thus, the inability of ISIS 113715 to reduce PTP1B expression by no more than 60% in whole liver as seen in previous experiments may result from a combination of a relatively high expression of PTP1B in NP cells with a reduced ability of ISIS 113715 to inhibit expression in this same cell fraction. Consequently, distinct targeting of the compound to hepatocytes, the key metabolic cell type in liver, results in a much greater inhibition of PTP1B levels.

Example 26

Effects of Antisense Inhibition of PTP1B Expression (ISIS 113715) in the Obese Insulin-Resistant Hyperinsulinemic Rhesus Monkey-Improved Insulin Sensitivity

In a further embodiment, male obese insulin-resistant hyperinsulinemic Rhesus monkeys were treated with ISIS 113715 (SEQ ID NO: 166) and insulin sensitivity, glucose tolerance and PTP1B mRNA and protein were measured. Serum samples were also measured for insulin levels.

Male rhesus monkeys were divided into two treatment groups, control animals (n=4; saline treatment only) and treated animals (n=8; treated with ISIS 113715). All animals had two pre-dosing glucose tolerance tests (GTTs) performed to establish insulin and glucose baseline values. Animals in the treatment group were dosed subcutaneously at a dose of 20 mg/kg (3 injections on alternate days the first week followed by one injection per week for the next two weeks). Fasted glucose/insulin levels and glucose tolerance (IVGTTs) were measured as pharmacologic endpoints.

As compared to baseline values, a 50% reduction in fasting insulin levels was observed (treated: 31.+-.9 vs. baseline: 67.+-.7 .mu.U/mL, p=0.0001), which was not accompanied by any change in plasma glucose levels. Furthermore, a marked reduction in insulin levels (AUC) was observed after IVGTTs (treated: 7295.+-.3178 vs. baseline: 18968.+-.2113 .mu.U-min/mL, p=0.0002). Insulin sensitivity was also significantly increased (glucose slope/insulin AUC; 5-20 minutes).

Hypoglycemia was not observed, even in the 16 hour-fasted animals. Levels of the liver enzymes ALT and AST were measured weekly and showed no change, indicating no ongoing toxic effects of the oligonucleotide treatment. Renal function tests were also normal.

The results of this study are consistent with those seen in previous rodent and monkey studies described herein which demonstrate a significant lowering of insulin levels suggesting that insulin efficiency (sensitivity) was increased upon treatment with ISIS 113715.

Example 27

RNA Synthesis

In general, RNA synthesis chemistry is based on the selective incorporation of various protecting groups at strategic intermediary reactions. Although one of ordinary skill in the art will understand the use of protecting groups in organic synthesis, a useful class of protecting groups includes silyl ethers. In particular bulky silyl ethers are used to protect the 5'-hydroxyl in combination with an acid-labile orthoester protecting group on the 2'-hydroxyl. This set of protecting groups is then used with standard solid-phase synthesis technology. It is important to lastly remove the acid labile orthoester protecting group after all other synthetic steps. Moreover, the early use of the silyl protecting groups during synthesis ensures facile removal when desired, without undesired deprotection of 2'hydroxyl.

Following this procedure for the sequential protection of the 5'-hydroxyl in combination with protection of the 2'-hydroxyl by protecting groups that are differentially removed and are differentially chemically labile, RNA oligonucleotides were synthesized.

RNA oligonucleotides are synthesized in a stepwise fashion. Each nucleotide is added sequentially (3'- to 5'-direction) to a solid support-bound oligonucleotide. The first nucleoside at the 3'-end of the chain is covalently attached to a solid support. The nucleotide precursor, a ribonucleoside phosphoramidite, and activator are added, coupling the second base onto the 5'-end of the first nucleoside. The support is washed and any unreacted 5'-hydroxyl groups are capped with acetic anhydride to yield 5'-acetyl moieties. The linkage is then oxidized to the more stable and ultimately desired P(V) linkage. At the end of the nucleotide addition cycle, the 5'-silyl group is cleaved with fluoride. The cycle is repeated for each subsequent nucleotide.

Following synthesis, the methyl protecting groups on the phosphates are cleaved in 30 minutes utilizing 1 M disodium-2-carbamoyl-2-cyanoethylene-1,1-dithiolate trihydrate (S.sub.2Na.sub.2) in DMF. The deprotection solution is washed from the solid support-bound oligonucleotide using water. The support is then treated with 40% methylamine in water for 10 minutes at 55.degree. C. This releases the RNA oligonucleotides into solution, deprotects the exocyclic amines, and modifies the 2'-groups. The oligonucleotides can be analyzed by anion exchange HPLC at this stage.

The 2'-orthoester groups are the last protecting groups to be removed. The ethylene glycol monoacetate orthoester protecting group developed by Dharmacon Research, Inc. (Lafayette, Colo.), is one example of a useful orthoester protecting group, which has the following important properties. It is stable to the conditions of nucleoside phosphoramidite synthesis and oligonucleotide synthesis. However, after oligonucleotide synthesis the oligonucleotide is treated with methylamine, which not only cleaves the oligonucleotide from the solid support but also removes the acetyl groups from the orthoesters. The resulting 2-ethyl-hydroxyl substituents on the orthoester are less electron withdrawing than the acetylated precursor. As a result, the modified orthoester becomes more labile to acid-catalyzed hydrolysis. Specifically, the rate of cleavage is approximately 10 times faster after the acetyl groups are removed. Therefore, this orthoester possesses sufficient stability in order to be compatible with oligonucleotide synthesis. Yet, when subsequently modified, it permits deprotection to be carried out under relatively mild aqueous conditions compatible with the final RNA oligonucleotide product.

Additionally, methods of RNA synthesis are well known in the art (Scaringe, S. A. Ph.D. Thesis, University of Colorado, 1996; Scaringe, S. A., et al., J. Am. Chem. Soc., 1998, 120, 11820-11821; Matteucci, M. D. and Caruthers, M. H. J. Am. Chem. Soc., 1981, 103, 3185-3191; Beaucage, S. L. and Caruthers, M. H. Tetrahedron Lett., 1981, 22, 1859-1862; Dahl, B. J., et al., Acta Chem. Scand., 1990, 44, 639-641; Reddy, M. P., et al., Tetrahedron Lett., 1994, 25, 4311-4314; Wincott, F. et al., Nucleic Acids Res., 1995, 23, 2677-2684; Griffin, B. E., et al., Tetrahedron, 1967, 23, 2301-2313; Griffin, B. E., et al., Tetrahedron, 1967, 23, 2315-2331).

RNA antisense compounds (RNA oligonucleotides) of the present invention can be synthesized by the methods herein or purchased from Dharmacon Research, Inc (Lafayette, Colo.). Once synthesized, complementary RNA antisense compounds can then be annealed by methods known in the art to form double stranded (duplexed) antisense compounds. For example, duplexes can be formed by combining 30 .mu.l of each of the complementary strands of RNA oligonucleotides (50 .mu.M RNA oligonucleotide solution) and 15 .mu.l of 5.times. annealing buffer (100 mM potassium acetate, 30 mM HEPES-KOH pH 7.4, 2 mM magnesium acetate) followed by heating for 1 minute at 90.degree. C., then 1 hour at 37.degree. C. The resulting duplexed antisense compounds can be used in kits, assays, screens, or other methods to investigate the role of a target nucleic acid.

Example 28

Design and Screening of Duplexed Antisense Compounds Targeting PTP1B

In accordance with the present invention, a series of nucleic acid duplexes comprising the antisense compounds of the present invention and their complements can be designed to target PTP1B. The nucleobase sequence of the antisense strand of the duplex comprises at least a portion of an oligonucleotide in Table 1. The ends of the strands may be modified by the addition of one or more natural or modified nucleobases to form an overhang. The sense strand of the dsRNA is then designed and synthesized as the complement of the antisense strand and may also contain modifications or additions to either terminus. For example, in one embodiment, both strands of the dsRNA duplex would be complementary over the central nucleobases, each having overhangs at one or both termini.

For example, a duplex comprising an antisense strand having the sequence CGAGAGGCGGACGGGACCG (nucleotides 1-19 of SEQ ID NO: 414) and having a two-nucleobase overhang of deoxythymidine (dT) would have the following structure:

##STR00001##

The one or more nucleobases forming the single-stranded overhang(s) may be dT as shown or may be another modified or unmodified nucleobase.

A duplex comprising an antisense strand having the sequence CGAGAGGCGGACGGGACCG (nucleotides 1-19 of SEQ ID NO: 414) may also prepared with blunt ends (no single stranded overhang) as shown (antisense strand below is nucleotides 1-19 of SEQ ID NO: 414; complement below is nucleotides 1-19 of SEQ ID NO: 415):

##STR00002##

RNA strands of the duplex can be synthesized by methods disclosed herein or purchased from Dharmacon Research Inc., (Lafayette, Colo.). Once synthesized, the complementary strands are annealed. The single strands are aliquoted and diluted to a concentration of 50 .mu.M. Once diluted, 30 .mu.L of each strand is combined with 15 .mu.L of a 5.times. solution of annealing buffer. The final concentration of said buffer is 100 mM potassium acetate, 30 mM HEPES-KOH pH 7.4, and 2 mM magnesium acetate. The final volume is 754. This solution is incubated for 1 minute at 90.degree. C. and then centrifuged for 15 seconds. The tube is allowed to sit for 1 hour at 37.degree. C. at which time the dsRNA duplexes are used in experimentation. The final concentration of the dsRNA duplex is 20 .mu.M. This solution can be stored frozen (-20.degree. C.) and freeze-thawed up to 5 times.

Once prepared, the duplexed antisense compounds are evaluated for their ability to modulate PTP1B expression. When cells reached 80% confluency, they are treated with duplexed antisense compounds of the invention. For cells grown in 96-well plates, wells are washed once with 200 .mu.L OPTI-MEM.TM.-1 reduced-serum medium (Gibco BRL) and then treated with 130 .mu.L of OPTI-MEM.TM.-1 medium containing 12 .mu.g/mL LIPOFECTIN.TM. reagent (Gibco BRL) and the desired duplex antisense compound at a final concentration of 200 nM. After 5 hours of treatment, the medium is replaced with fresh medium. Cells are harvested 16 hours after treatment, at which time RNA is isolated and target reduction measured by RT-PCR.

A series of siRNA duplexes were prepared as described above and were tested in A549 cells for their ability to reduce human PTP1b expression. Also tested for comparison were several single-stranded 2'-MOE gapped (chimeric) oligonucleotides as well as two single-stranded controls (ISIS 116847, targeted to PTEN, and ISIS 129700, a scrambled control) and two RNA duplex unrelated controls (ISIS 271783:ISIS 297802 duplex and ISIS 263188:263189 duplex), which are targeted to PTEN. These compounds were tested at two concentrations, 75 nM and 150 nM. The results are shown in Table 5.

TABLE-US-00005 TABLE 5 Inhibition of human PTP1B expression by siRNA duplexes Isis No. Anti-sense Sense Target anti- strand Strand site on % % sense: SEQ ID SEQ ID SEQ ID Inhib7 Inhib7 Chem- sense Antisense strand sequence NO NO NO: 3 5 nM 150 nM istry.sup.1 348290: UUCAUGUCGGAUAUCCUGGdTdA 390 403 148 53 70 R 348274 348291: UCACUGGCUUCAUGUCGGAdTdA 391 404 156 0 12 R 348275 348292: GGUAAGAAUGUAACUCCUUdTdG 392 405 322 8 9 R 348276 348293: CUUCAGAGAUCAAUGUUAAdTdT 393 406 512 0 28 R 348277 348294: UAGCUGUCGCACUGUAUAAdTdA 394 407 544 44 52 R 348278 348295: CCAAUUCUAGCUGUCGCACdTdG 395 408 551 67 79 R 348279 342914: UUGAUAAAGCCCUUGAUGCA 396 409 1884 66 80 R 342934 342916: GGUCAUGCACAGGCAGGUUG 397 410 2274 55 72 R 342936 342908: GAAGAAGGGUCUUUCCUCUU 398 411 799 61 77 R 342928 107772 CCCGGACTTGTCGATCTGCT 20 N/A 113 76 90 G 107804 CAGTGTCTTGACTCATGCTT 52 N/A 1176 85 95 G 107813 CCGCGGCATGCCTGCTAGTC 61 N/A 1460 71 88 G 107831 GGTCATGCACAGGCAGGTTG 79 N/A 2274 83 88 G 116847 CTGCTAGCCTCTGGATTTGA 399 N/A N/A 0 0 G 129700 TAGTGCGGACCTACCCACGA 400 N/A N/A 17 13 G 271783: GGGACGAACUGGUGUAAUGdTdT 401 412 N/A 0 4 R 297802 263188: CUUCUGGCAUCCGGUUUAGdTdT 402 413 N/A 28 9 R 263189 .sup.1Chemistry: "R" indicates an RNA duplex in which both strands are 2' ribonucleic acid, except where 2' deoxynucleotides are indicated by a "d" preceding the base. All linkages are P = S. "G" indicates a single-stranded 2' MOE gapmer in which nucleotides 1-5 and 16-20 are 2' MOE nucleotides and nucleotides 6-15 are 2'-deoxy. All linkages are P = S and all cytosines are 5-methylcytosines.

As can be seen from the data in Table 5, both siRNA duplexes and single stranded 2'MOE gapped oligonucleotides inhibit human PTP1b target expression in a dose-dependent manner.

SEQUENCE LISTINGS

1

415120DNAArtificial SequenceSynthetic Oligonucleotide 1tccgtcatcg ctcctcaggg 20220DNAArtificial SequenceSynthetic Oligonucleotide 2atgcattctg cccccaagga 2033247DNAHomo sapiensCDS(91)...(1398) 3gggcgggcct cggggctaag agcgcgacgc ctagagcggc agacggcgca gtgggccgag 60aaggaggcgc agcagccgcc ctggcccgtc atg gag atg gaa aag gag ttc gag 114 Met Glu Met Glu Lys Glu Phe Glu 1 5cag atc gac aag tcc ggg agc tgg gcg gcc att tac cag gat atc cga 162Gln Ile Asp Lys Ser Gly Ser Trp Ala Ala Ile Tyr Gln Asp Ile Arg 10 15 20cat gaa gcc agt gac ttc cca tgt aga gtg gcc aag ctt cct aag aac 210His Glu Ala Ser Asp Phe Pro Cys Arg Val Ala Lys Leu Pro Lys Asn 25 30 35 40aaa aac cga aat agg tac aga gac gtc agt ccc ttt gac cat agt cgg 258Lys Asn Arg Asn Arg Tyr Arg Asp Val Ser Pro Phe Asp His Ser Arg 45 50 55att aaa cta cat caa gaa gat aat gac tat atc aac gct agt ttg ata 306Ile Lys Leu His Gln Glu Asp Asn Asp Tyr Ile Asn Ala Ser Leu Ile 60 65 70aaa atg gaa gaa gcc caa agg agt tac att ctt acc cag ggc cct ttg 354Lys Met Glu Glu Ala Gln Arg Ser Tyr Ile Leu Thr Gln Gly Pro Leu 75 80 85cct aac aca tgc ggt cac ttt tgg gag atg gtg tgg gag cag aaa agc 402Pro Asn Thr Cys Gly His Phe Trp Glu Met Val Trp Glu Gln Lys Ser 90 95 100agg ggt gtc gtc atg ctc aac aga gtg atg gag aaa ggt tcg tta aaa 450Arg Gly Val Val Met Leu Asn Arg Val Met Glu Lys Gly Ser Leu Lys105 110 115 120tgc gca caa tac tgg cca caa aaa gaa gaa aaa gag atg atc ttt gaa 498Cys Ala Gln Tyr Trp Pro Gln Lys Glu Glu Lys Glu Met Ile Phe Glu 125 130 135gac aca aat ttg aaa tta aca ttg atc tct gaa gat atc aag tca tat 546Asp Thr Asn Leu Lys Leu Thr Leu Ile Ser Glu Asp Ile Lys Ser Tyr 140 145 150tat aca gtg cga cag cta gaa ttg gaa aac ctt aca acc caa gaa act 594Tyr Thr Val Arg Gln Leu Glu Leu Glu Asn Leu Thr Thr Gln Glu Thr 155 160 165cga gag atc tta cat ttc cac tat acc aca tgg cct gac ttt gga gtc 642Arg Glu Ile Leu His Phe His Tyr Thr Thr Trp Pro Asp Phe Gly Val 170 175 180cct gaa tca cca gcc tca ttc ttg aac ttt ctt ttc aaa gtc cga gag 690Pro Glu Ser Pro Ala Ser Phe Leu Asn Phe Leu Phe Lys Val Arg Glu185 190 195 200tca ggg tca ctc agc ccg gag cac ggg ccc gtt gtg gtg cac tgc agt 738Ser Gly Ser Leu Ser Pro Glu His Gly Pro Val Val Val His Cys Ser 205 210 215gca ggc atc ggc agg tct gga acc ttc tgt ctg gct gat acc tgc ctc 786Ala Gly Ile Gly Arg Ser Gly Thr Phe Cys Leu Ala Asp Thr Cys Leu 220 225 230ctg ctg atg gac aag agg aaa gac cct tct tcc gtt gat atc aag aaa 834Leu Leu Met Asp Lys Arg Lys Asp Pro Ser Ser Val Asp Ile Lys Lys 235 240 245gtg ctg tta gaa atg agg aag ttt cgg atg ggg ttg atc cag aca gcc 882Val Leu Leu Glu Met Arg Lys Phe Arg Met Gly Leu Ile Gln Thr Ala 250 255 260gac cag ctg cgc ttc tcc tac ctg gct gtg atc gaa ggt gcc aaa ttc 930Asp Gln Leu Arg Phe Ser Tyr Leu Ala Val Ile Glu Gly Ala Lys Phe265 270 275 280atc atg ggg gac tct tcc gtg cag gat cag tgg aag gag ctt tcc cac 978Ile Met Gly Asp Ser Ser Val Gln Asp Gln Trp Lys Glu Leu Ser His 285 290 295gag gac ctg gag ccc cca ccc gag cat atc ccc cca cct ccc cgg cca 1026Glu Asp Leu Glu Pro Pro Pro Glu His Ile Pro Pro Pro Pro Arg Pro 300 305 310ccc aaa cga atc ctg gag cca cac aat ggg aaa tgc agg gag ttc ttc 1074Pro Lys Arg Ile Leu Glu Pro His Asn Gly Lys Cys Arg Glu Phe Phe 315 320 325cca aat cac cag tgg gtg aag gaa gag acc cag gag gat aaa gac tgc 1122Pro Asn His Gln Trp Val Lys Glu Glu Thr Gln Glu Asp Lys Asp Cys 330 335 340ccc atc aag gaa gaa aaa gga agc ccc tta aat gcc gca ccc tac ggc 1170Pro Ile Lys Glu Glu Lys Gly Ser Pro Leu Asn Ala Ala Pro Tyr Gly345 350 355 360atc gaa agc atg agt caa gac act gaa gtt aga agt cgg gtc gtg ggg 1218Ile Glu Ser Met Ser Gln Asp Thr Glu Val Arg Ser Arg Val Val Gly 365 370 375gga agt ctt cga ggt gcc cag gct gcc tcc cca gcc aaa ggg gag ccg 1266Gly Ser Leu Arg Gly Ala Gln Ala Ala Ser Pro Ala Lys Gly Glu Pro 380 385 390tca ctg ccc gag aag gac gag gac cat gca ctg agt tac tgg aag ccc 1314Ser Leu Pro Glu Lys Asp Glu Asp His Ala Leu Ser Tyr Trp Lys Pro 395 400 405ttc ctg gtc aac atg tgc gtg gct acg gtc ctc acg gcc ggc gct tac 1362Phe Leu Val Asn Met Cys Val Ala Thr Val Leu Thr Ala Gly Ala Tyr 410 415 420ctc tgc tac agg ttc ctg ttc aac agc aac aca tag cctgaccctc 1408Leu Cys Tyr Arg Phe Leu Phe Asn Ser Asn Thr425 430 435ctccactcca cctccaccca ctgtccgcct ctgcccgcag agcccacgcc cgactagcag 1468gcatgccgcg gtaggtaagg gccgccggac cgcgtagaga gccgggcccc ggacggacgt 1528tggttctgca ctaaaaccca tcttccccgg atgtgtgtct cacccctcat ccttttactt 1588tttgcccctt ccactttgag taccaaatcc acaagccatt ttttgaggag agtgaaagag 1648agtaccatgc tggcggcgca gagggaaggg gcctacaccc gtcttggggc tcgccccacc 1708cagggctccc tcctggagca tcccaggcgg cgcacgccaa cagccccccc cttgaatctg 1768cagggagcaa ctctccactc catatttatt taaacaattt tttccccaaa ggcatccata 1828gtgcactagc attttcttga accaataatg tattaaaatt ttttgatgtc agccttgcat 1888caagggcttt atcaaaaagt acaataataa atcctcaggt agtactggga atggaaggct 1948ttgccatggg cctgctgcgt cagaccagta ctgggaagga ggacggttgt aagcagttgt 2008tatttagtga tattgtgggt aacgtgagaa gatagaacaa tgctataata tataatgaac 2068acgtgggtat ttaataagaa acatgatgtg agattacttt gtcccgctta ttctcctccc 2128tgttatctgc tagatctagt tctcaatcac tgctcccccg tgtgtattag aatgcatgta 2188aggtcttctt gtgtcctgat gaaaaatatg tgcttgaaat gagaaacttt gatctctgct 2248tactaatgtg ccccatgtcc aagtccaacc tgcctgtgca tgacctgatc attacatggc 2308tgtggttcct aagcctgttg ctgaagtcat tgtcgctcag caatagggtg cagttttcca 2368ggaataggca tttgctaatt cctggcatga cactctagtg acttcctggt gaggcccagc 2428ctgtcctggt acagcagggt cttgctgtaa ctcagacatt ccaagggtat gggaagccat 2488attcacacct cacgctctgg acatgattta gggaagcagg gacacccccc gccccccacc 2548tttgggatca gcctccgcca ttccaagtca acactcttct tgagcagacc gtgatttgga 2608agagaggcac ctgctggaaa ccacacttct tgaaacagcc tgggtgacgg tcctttaggc 2668agcctgccgc cgtctctgtc ccggttcacc ttgccgagag aggcgcgtct gccccaccct 2728caaaccctgt ggggcctgat ggtgctcacg actcttcctg caaagggaac tgaagacctc 2788cacattaagt ggctttttaa catgaaaaac acggcagctg tagctcccga gctactctct 2848tgccagcatt ttcacatttt gcctttctcg tggtagaagc cagtacagag aaattctgtg 2908gtgggaacat tcgaggtgtc accctgcaga gctatggtga ggtgtggata aggcttaggt 2968gccaggctgt aagcattctg agctggcttg ttgtttttaa gtcctgtata tgtatgtagt 3028agtttgggtg tgtatatata gtagcatttc aaaatggacg tactggttta acctcctatc 3088cttggagagc agctggctct ccaccttgtt acacattatg ttagagaggt agcgagctgc 3148tctgctatat gccttaagcc aatatttact catcaggtca ttatttttta caatggccat 3208ggaataaacc atttttacaa aaataaaaac aaaaaaagc 3247421DNAArtificial SequencePCR Primer 4ggagttcgag cagatcgaca a 21521DNAArtificial SequencePCR Primer 5ggccactcta catgggaagt c 21624DNAArtificial SequencePCR Probe 6agctgggcgg ccatttacca ggat 24719DNAArtificial SequencePCR Primer 7gaaggtgaag gtcggagtc 19820DNAArtificial SequencePCR Primer 8gaagatggtg atgggatttc 20920DNAArtificial SequencePCR Probe 9caagcttccc gttctcagcc 20104127DNARattus norvegicusCDS(120)...(1418) 10agccgctgct ggggaggttg gggctgaggt ggtggcgggc gacgggcctc gagacgcgga 60gcgacgcggc ctagcgcggc ggacggccga gggaactcgg gcagtcgtcc cgtcccgcc 119atg gaa atg gag aag gaa ttc gag cag atc gat aag gct ggg aac tgg 167Met Glu Met Glu Lys Glu Phe Glu Gln Ile Asp Lys Ala Gly Asn Trp 1 5 10 15gcg gct att tac cag gat att cga cat gaa gcc agt gac ttc cca tgc 215Ala Ala Ile Tyr Gln Asp Ile Arg His Glu Ala Ser Asp Phe Pro Cys 20 25 30aga ata gcg aaa ctt cct aag aac aaa aac cgg aac agg tac cga gat 263Arg Ile Ala Lys Leu Pro Lys Asn Lys Asn Arg Asn Arg Tyr Arg Asp 35 40 45gtc agc cct ttt gac cac agt cgg att aaa ttg cat cag gaa gat aat 311Val Ser Pro Phe Asp His Ser Arg Ile Lys Leu His Gln Glu Asp Asn 50 55 60gac tat atc aat gcc agc ttg ata aaa atg gag gaa gcc cag agg agc 359Asp Tyr Ile Asn Ala Ser Leu Ile Lys Met Glu Glu Ala Gln Arg Ser 65 70 75 80tat atc ctc acc cag ggc cct tta cca aac acg tgc ggg cac ttc tgg 407Tyr Ile Leu Thr Gln Gly Pro Leu Pro Asn Thr Cys Gly His Phe Trp 85 90 95gag atg gtg tgg gag cag aag agc agg ggc gtg gtc atg ctc aac cgc 455Glu Met Val Trp Glu Gln Lys Ser Arg Gly Val Val Met Leu Asn Arg 100 105 110atc atg gag aaa ggc tcg tta aaa tgt gcc cag tat tgg cca cag aaa 503Ile Met Glu Lys Gly Ser Leu Lys Cys Ala Gln Tyr Trp Pro Gln Lys 115 120 125gaa gaa aaa gag atg gtc ttc gat gac acc aat ttg aag ctg aca ctg 551Glu Glu Lys Glu Met Val Phe Asp Asp Thr Asn Leu Lys Leu Thr Leu 130 135 140atc tct gaa gat gtc aag tca tat tac aca gta cgg cag ttg gag ttg 599Ile Ser Glu Asp Val Lys Ser Tyr Tyr Thr Val Arg Gln Leu Glu Leu145 150 155 160gag aac ctg gct acc cag gag gct cga gag atc ctg cat ttc cac tac 647Glu Asn Leu Ala Thr Gln Glu Ala Arg Glu Ile Leu His Phe His Tyr 165 170 175acc acc tgg cct gac ttt gga gtc cct gag tca cct gcc tct ttc ctc 695Thr Thr Trp Pro Asp Phe Gly Val Pro Glu Ser Pro Ala Ser Phe Leu 180 185 190aat ttc cta ttc aaa gtc cga gag tca ggc tca ctc agc cca gag cac 743Asn Phe Leu Phe Lys Val Arg Glu Ser Gly Ser Leu Ser Pro Glu His 195 200 205ggc ccc att gtg gtc cac tgc agt gct ggc att ggc agg tca ggg acc 791Gly Pro Ile Val Val His Cys Ser Ala Gly Ile Gly Arg Ser Gly Thr 210 215 220ttc tgc ctg gct gac acc tgc ctc tta ctg atg gac aag agg aaa gac 839Phe Cys Leu Ala Asp Thr Cys Leu Leu Leu Met Asp Lys Arg Lys Asp225 230 235 240ccg tcc tct gtg gac atc aag aaa gtg ctg ttg gag atg cgc agg ttc 887Pro Ser Ser Val Asp Ile Lys Lys Val Leu Leu Glu Met Arg Arg Phe 245 250 255cgc atg ggg ctc atc cag acg gcc gac caa ctg cgc ttc tcc tac ctg 935Arg Met Gly Leu Ile Gln Thr Ala Asp Gln Leu Arg Phe Ser Tyr Leu 260 265 270gct gtg atc gag ggt gca aag ttc atc atg ggc gac tcg tca gtg cag 983Ala Val Ile Glu Gly Ala Lys Phe Ile Met Gly Asp Ser Ser Val Gln 275 280 285gat cag tgg aag gag ctt tcc cat gaa gac ctg gag cct ccc cct gag 1031Asp Gln Trp Lys Glu Leu Ser His Glu Asp Leu Glu Pro Pro Pro Glu 290 295 300cac gtg ccc cca cct ccc cgg cca ccc aaa cgc aca ttg gag cct cac 1079His Val Pro Pro Pro Pro Arg Pro Pro Lys Arg Thr Leu Glu Pro His305 310 315 320aat ggc aag tgc aag gag ctc ttc tcc aac cac cag tgg gtg agc gag 1127Asn Gly Lys Cys Lys Glu Leu Phe Ser Asn His Gln Trp Val Ser Glu 325 330 335gag agc tgt gag gat gag gac atc ctg gcc aga gag gaa agc aga gcc 1175Glu Ser Cys Glu Asp Glu Asp Ile Leu Ala Arg Glu Glu Ser Arg Ala 340 345 350ccc tca att gct gtg cac agc atg agc agt atg agt caa gac act gaa 1223Pro Ser Ile Ala Val His Ser Met Ser Ser Met Ser Gln Asp Thr Glu 355 360 365gtt agg aaa cgg atg gtg ggt gga ggt ctt caa agt gct cag gca tct 1271Val Arg Lys Arg Met Val Gly Gly Gly Leu Gln Ser Ala Gln Ala Ser 370 375 380gtc ccc act gag gaa gag ctg tcc cca acc gag gag gaa caa aag gca 1319Val Pro Thr Glu Glu Glu Leu Ser Pro Thr Glu Glu Glu Gln Lys Ala385 390 395 400cac agg cca gtt cac tgg aag ccc ttc ctg gtc aac gtg tgc atg gcc 1367His Arg Pro Val His Trp Lys Pro Phe Leu Val Asn Val Cys Met Ala 405 410 415acg gcc ctg gcg act ggc gcg tac ctc tgt tac cgg gta tgt ttt cac 1415Thr Ala Leu Ala Thr Gly Ala Tyr Leu Cys Tyr Arg Val Cys Phe His 420 425 430tga cagactgctg tgaggcatga gcgtggtggg cgctgccact gcccaggtta 1468ggatttggtc tgcggcgtct aacctggtgt agaagaaaca acagcttaca agcctgtggt 1528ggaactggaa gggccagccc caggaggggc atctgtgcac tgggctttga aggagcccct 1588ggtcccaaga acagagtcta atctcagggc cttaacctgt tcaggagaag tagaggaaat 1648gccaaatact cttcttgctc tcacctcact cctccccttt ctctggttcg tttgtttttg 1708gaaaaaaaaa aaaaagaatt acaacacatt gttgttttta acatttataa aggcaggttt 1768ttgttatttt tagagaaaac aaaagatgct aggcactggt gagattctct tgtgcccttt 1828ggcatgtgat cagattcacg atttacgttt atttccgggg gagggtccca cctgtcagga 1888ctgtaaagtt cctgctggct tggtcagccc ccccaccccc ccaccccgag cttgcaggtg 1948ccctgctgtg aggagagcag cagcagaggc tgcccctgga cagaagccca gctctgcttc 2008cctcaggtgt ccctgcgttt ccatcctcct tctttgtgac cgccatcttg cagatgaccc 2068agtcctcagc accccacccc tgcagatggg tttctccgag ggcctgcctc agggtcatca 2128gaggttggct gccagcttag agctggggct tccatttgat tggaaagtca ttactattct 2188atgtagaagc cactccactg aggtgtaaag caagactcat aaaggaggag ccttggtgtc 2248atggaagtca ctccgcgcgc aggacctgta acaacctctg aaacactcag tcctgctgca 2308gtgacgtcct tgaaggcatc agacagatga tttgcagact gccaagactt gtcctgagcc 2368gtgattttta gagtctggac tcatgaaaca ccgccgagcg cttactgtgc agcctctgat 2428gctggttggc tgaggctgcg gggaggtgga cactgtgggt gcatccagtg cagttgcttt 2488tgtgcagttg ggtccagcag cacagcccgc actccagcct cagctgcagg ccacagtggc 2548catggaggcc gccagagcga gctggggtgg atgcttgttc acttggagca gccttcccag 2608gacgtgcagc tcccttcctg ctttgtcctt ctgcttcctt ccctggagta gcaagcccac 2668gagcaatcgt gaggggtgtg agggagctgc agaggcatca gagtggcctg cagcggcgtg 2728aggccccttc ccctccgaca cccccctcca gaggagccgc tccactgtta tttattcact 2788ttgcccacag acacccctga gtgagcacac cctgaaactg accgtgtaag gtgtcagcct 2848gcacccagga ccgtcaggtg cagcaccggg tcagtcctag ggttgaggta ggactgacac 2908agccactgtg tggctggtgc tggggcaggg gcaggagctg agggtcttag aagcaatctt 2968caggaacaga caacagtggt gacatgtaaa gtccctgtgg ctactgatga catgtgtagg 3028atgaaggctg gcctttctcc catgactttc tagatcccgt tccccgtctg ctttccctgt 3088gagttagaaa acacacaggc tcctgtcctg gtggtgccgt gtgcttgaca tgggaaactt 3148agatgcctgc tcactggcgg gcacctcggc atcgccacca ctcagagtga gagcagtgct 3208gtccagtgcc gaggccgcct gactcccggc aggactcttc aggctctggc ctgccccagc 3268acaccccgct ggatctcaga cattccacac ccacacctca ttccctggac acttgggcaa 3328gcaggcccgc ccttccacct ctggggtcag cccctccatt ccgagttcac actgctctgg 3388agcaggccag gaccggaagc aaggcagctg gtgaggagca ccctcctggg aacagtgtag 3448gtgacagtcc tgagagtcag cttgctagcg ctgctggcac cagtcacctt gctcagaagt 3508gtgtggctct tgaggctgaa gagactgatg atggtgctca tgactcttct gtgaggggaa 3568cttgaccttc acattgggtg gcttttttta aaataagcga aggcagctgg aactccagtc 3628tgcctcttgc cagcacttca cattttgcct ttcacccaga gaagccagca cagagccact 3688ggggaaggcg atggccttgc ctgcacaggc tgaggagatg gctcagccgg cgtccaggct 3748gtgtctggag cagggggtgc acagcagcct cacaggtggg ggcctcagag caggcgctgc 3808cctgtcccct gccccgctgg aggcagcaaa gctgctgcat gccttaagtc aatacttact 3868cagcagggcg ctctcgttct ctctctctct ctctctctct ctctctctct ctctctctct 3928ctctctaaat ggccatagaa taaaccattt tacaaaaata aaagccaaca acaaagtgct 3988ctggaatagc acctttgcag gagcgggggg tgtctcaggg tcttctgtga cctcaccgaa 4048ctgtccgact gcaccgtttc caacttgtgt ctcactaatg ggtctgcatt agttgcaaca 4108ataaatgttt ttaaagaac 41271121DNAArtificial SequencePCR Primer 11cgagggtgca aagttcatca t 211221DNAArtificial SequencePCR Primer 12ccaggtcttc atgggaaagc t 211326DNAArtificial SequencePCR Probe 13cgactcgtca gtgcaggatc agtgga 261423DNAArtificial SequencePCR Primer 14tgttctagag acagccgcat ctt 231521DNAArtificial SequencePCR Primer 15caccgacctt caccatcttg t 211624DNAArtificial SequencePCR Probe 16ttgtgcagtg ccagcctcgt ctca 241720DNAArtificial SequenceSynthetic Oligonucleotide 17cttagccccg aggcccgccc 201820DNAArtificial SequenceSynthetic Oligonucleotide 18ctcggcccac tgcgccgtct 201920DNAArtificial SequenceSynthetic Oligonucleotide 19catgacgggc

cagggcggct 202020DNAArtificial SequenceSynthetic Oligonucleotide 20cccggacttg tcgatctgct 202120DNAArtificial SequenceSynthetic Oligonucleotide 21ctggcttcat gtcggatatc 202220DNAArtificial SequenceSynthetic Oligonucleotide 22ttggccactc tacatgggaa 202320DNAArtificial SequenceSynthetic Oligonucleotide 23ggactgacgt ctctgtacct 202420DNAArtificial SequenceSynthetic Oligonucleotide 24gatgtagttt aatccgacta 202520DNAArtificial SequenceSynthetic Oligonucleotide 25ctagcgttga tatagtcatt 202620DNAArtificial SequenceSynthetic Oligonucleotide 26gggtaagaat gtaactcctt 202720DNAArtificial SequenceSynthetic Oligonucleotide 27tgaccgcatg tgttaggcaa 202820DNAArtificial SequenceSynthetic Oligonucleotide 28ttttctgctc ccacaccatc 202920DNAArtificial SequenceSynthetic Oligonucleotide 29ctctgttgag catgacgaca 203020DNAArtificial SequenceSynthetic Oligonucleotide 30gcgcatttta acgaaccttt 203120DNAArtificial SequenceSynthetic Oligonucleotide 31aaatttgtgt cttcaaagat 203220DNAArtificial SequenceSynthetic Oligonucleotide 32tgatatcttc agagatcaat 203320DNAArtificial SequenceSynthetic Oligonucleotide 33tctagctgtc gcactgtata 203420DNAArtificial SequenceSynthetic Oligonucleotide 34agtttcttgg gttgtaaggt 203520DNAArtificial SequenceSynthetic Oligonucleotide 35gtggtatagt ggaaatgtaa 203620DNAArtificial SequenceSynthetic Oligonucleotide 36tgattcaggg actccaaagt 203720DNAArtificial SequenceSynthetic Oligonucleotide 37ttgaaaagaa agttcaagaa 203820DNAArtificial SequenceSynthetic Oligonucleotide 38gggctgagtg accctgactc 203920DNAArtificial SequenceSynthetic Oligonucleotide 39gcagtgcacc acaacgggcc 204020DNAArtificial SequenceSynthetic Oligonucleotide 40aggttccaga cctgccgatg 204120DNAArtificial SequenceSynthetic Oligonucleotide 41agcaggaggc aggtatcagc 204220DNAArtificial SequenceSynthetic Oligonucleotide 42gaagaagggt ctttcctctt 204320DNAArtificial SequenceSynthetic Oligonucleotide 43tctaacagca ctttcttgat 204420DNAArtificial SequenceSynthetic Oligonucleotide 44atcaacccca tccgaaactt 204520DNAArtificial SequenceSynthetic Oligonucleotide 45gagaagcgca gctggtcggc 204620DNAArtificial SequenceSynthetic Oligonucleotide 46tttggcacct tcgatcacag 204720DNAArtificial SequenceSynthetic Oligonucleotide 47agctccttcc actgatcctg 204820DNAArtificial SequenceSynthetic Oligonucleotide 48tccaggattc gtttgggtgg 204920DNAArtificial SequenceSynthetic Oligonucleotide 49gaactccctg catttcccat 205020DNAArtificial SequenceSynthetic Oligonucleotide 50ttccttcacc cactggtgat 205120DNAArtificial SequenceSynthetic Oligonucleotide 51gtagggtgcg gcatttaagg 205220DNAArtificial SequenceSynthetic Oligonucleotide 52cagtgtcttg actcatgctt 205320DNAArtificial SequenceSynthetic Oligonucleotide 53gcctgggcac ctcgaagact 205420DNAArtificial SequenceSynthetic Oligonucleotide 54ctcgtccttc tcgggcagtg 205520DNAArtificial SequenceSynthetic Oligonucleotide 55gggcttccag taactcagtg 205620DNAArtificial SequenceSynthetic Oligonucleotide 56ccgtagccac gcacatgttg 205720DNAArtificial SequenceSynthetic Oligonucleotide 57tagcagaggt aagcgccggc 205820DNAArtificial SequenceSynthetic Oligonucleotide 58ctatgtgttg ctgttgaaca 205920DNAArtificial SequenceSynthetic Oligonucleotide 59ggaggtggag tggaggaggg 206020DNAArtificial SequenceSynthetic Oligonucleotide 60ggctctgcgg gcagaggcgg 206120DNAArtificial SequenceSynthetic Oligonucleotide 61ccgcggcatg cctgctagtc 206220DNAArtificial SequenceSynthetic Oligonucleotide 62tctctacgcg gtccggcggc 206320DNAArtificial SequenceSynthetic Oligonucleotide 63aagatgggtt ttagtgcaga 206420DNAArtificial SequenceSynthetic Oligonucleotide 64gtactctctt tcactctcct 206520DNAArtificial SequenceSynthetic Oligonucleotide 65ggccccttcc ctctgcgccg 206620DNAArtificial SequenceSynthetic Oligonucleotide 66ctccaggagg gagccctggg 206720DNAArtificial SequenceSynthetic Oligonucleotide 67gggctgttgg cgtgcgccgc 206820DNAArtificial SequenceSynthetic Oligonucleotide 68tttaaataaa tatggagtgg 206920DNAArtificial SequenceSynthetic Oligonucleotide 69gttcaagaaa atgctagtgc 207020DNAArtificial SequenceSynthetic Oligonucleotide 70ttgataaagc ccttgatgca 207120DNAArtificial SequenceSynthetic Oligonucleotide 71atggcaaagc cttccattcc 207220DNAArtificial SequenceSynthetic Oligonucleotide 72gtcctccttc ccagtactgg 207320DNAArtificial SequenceSynthetic Oligonucleotide 73ttacccacaa tatcactaaa 207420DNAArtificial SequenceSynthetic Oligonucleotide 74attatatatt atagcattgt 207520DNAArtificial SequenceSynthetic Oligonucleotide 75tcacatcatg tttcttatta 207620DNAArtificial SequenceSynthetic Oligonucleotide 76ataacaggga ggagaataag 207720DNAArtificial SequenceSynthetic Oligonucleotide 77ttacatgcat tctaatacac 207820DNAArtificial SequenceSynthetic Oligonucleotide 78gatcaaagtt tctcatttca 207920DNAArtificial SequenceSynthetic Oligonucleotide 79ggtcatgcac aggcaggttg 208020DNAArtificial SequenceSynthetic Oligonucleotide 80caacaggctt aggaaccaca 208120DNAArtificial SequenceSynthetic Oligonucleotide 81aactgcaccc tattgctgag 208220DNAArtificial SequenceSynthetic Oligonucleotide 82gtcatgccag gaattagcaa 208320DNAArtificial SequenceSynthetic Oligonucleotide 83acaggctggg cctcaccagg 208420DNAArtificial SequenceSynthetic Oligonucleotide 84tgagttacag caagaccctg 208520DNAArtificial SequenceSynthetic Oligonucleotide 85gaatatggct tcccataccc 208620DNAArtificial SequenceSynthetic Oligonucleotide 86ccctaaatca tgtccagagc 208720DNAArtificial SequenceSynthetic Oligonucleotide 87gacttggaat ggcggaggct 208820DNAArtificial SequenceSynthetic Oligonucleotide 88caaatcacgg tctgctcaag 208920DNAArtificial SequenceSynthetic Oligonucleotide 89gaagtgtggt ttccagcagg 209020DNAArtificial SequenceSynthetic Oligonucleotide 90cctaaaggac cgtcacccag 209120DNAArtificial SequenceSynthetic Oligonucleotide 91gtgaaccggg acagagacgg 209220DNAArtificial SequenceSynthetic Oligonucleotide 92gccccacagg gtttgagggt 209320DNAArtificial SequenceSynthetic Oligonucleotide 93cctttgcagg aagagtcgtg 209420DNAArtificial SequenceSynthetic Oligonucleotide 94aaagccactt aatgtggagg 209520DNAArtificial SequenceSynthetic Oligonucleotide 95gtgaaaatgc tggcaagaga 209620DNAArtificial SequenceSynthetic Oligonucleotide 96tcagaatgct tacagcctgg 209720DNAArtificial SequenceSynthetic Oligonucleotide 97caacctcccc agcagcggct 209820DNAArtificial SequenceSynthetic Oligonucleotide 98tcgaggcccg tcgcccgcca 209920DNAArtificial SequenceSynthetic Oligonucleotide 99cctcggccgt ccgccgcgct 2010020DNAArtificial SequenceSynthetic Oligonucleotide 100tcgatctgct cgaattcctt 2010120DNAArtificial SequenceSynthetic Oligonucleotide 101cctggtaaat agccgcccag 2010220DNAArtificial SequenceSynthetic Oligonucleotide 102tgtcgaatat cctggtaaat 2010320DNAArtificial SequenceSynthetic Oligonucleotide 103actggcttca tgtcgaatat 2010420DNAArtificial SequenceSynthetic Oligonucleotide 104aagtcactgg cttcatgtcg 2010520DNAArtificial SequenceSynthetic Oligonucleotide 105gaagtcactg gcttcatgtc 2010620DNAArtificial SequenceSynthetic Oligonucleotide 106ggaagtcact ggcttcatgt 2010720DNAArtificial SequenceSynthetic Oligonucleotide 107gggaagtcac tggcttcatg 2010820DNAArtificial SequenceSynthetic Oligonucleotide 108tgggaagtca ctggcttcat 2010920DNAArtificial SequenceSynthetic Oligonucleotide 109atgggaagtc actggcttca 2011020DNAArtificial SequenceSynthetic Oligonucleotide 110catgggaagt cactggcttc 2011120DNAArtificial SequenceSynthetic Oligonucleotide 111tttttgttct taggaagttt 2011220DNAArtificial SequenceSynthetic Oligonucleotide 112cggtttttgt tcttaggaag 2011320DNAArtificial SequenceSynthetic Oligonucleotide 113tccgactgtg gtcaaaaggg 2011420DNAArtificial SequenceSynthetic Oligonucleotide 114ttaatccgac tgtggtcaaa 2011520DNAArtificial SequenceSynthetic Oligonucleotide 115atagtcatta tcttcctgat 2011620DNAArtificial SequenceSynthetic Oligonucleotide 116ttgatatagt cattatcttc 2011720DNAArtificial SequenceSynthetic Oligonucleotide 117gcttcctcca tttttatcaa 2011820DNAArtificial SequenceSynthetic Oligonucleotide 118ggccctgggt gaggatatag 2011920DNAArtificial SequenceSynthetic Oligonucleotide 119cacaccatct cccagaagtg 2012020DNAArtificial SequenceSynthetic Oligonucleotide 120tgctcccaca ccatctccca 2012120DNAArtificial SequenceSynthetic Oligonucleotide 121ctgctcccac accatctccc 2012220DNAArtificial SequenceSynthetic Oligonucleotide 122tctgctccca caccatctcc 2012320DNAArtificial SequenceSynthetic Oligonucleotide 123ttctgctccc acaccatctc 2012420DNAArtificial SequenceSynthetic Oligonucleotide 124cccctgctct tctgctccca 2012520DNAArtificial SequenceSynthetic Oligonucleotide 125atgcggttga gcatgaccac 2012620DNAArtificial SequenceSynthetic Oligonucleotide 126tttaacgagc ctttctccat 2012720DNAArtificial SequenceSynthetic Oligonucleotide 127ttttcttctt tctgtggcca 2012820DNAArtificial SequenceSynthetic Oligonucleotide 128gaccatctct ttttcttctt 2012920DNAArtificial SequenceSynthetic Oligonucleotide 129tcagagatca gtgtcagctt 2013020DNAArtificial SequenceSynthetic Oligonucleotide 130cttgacatct tcagagatca 2013120DNAArtificial SequenceSynthetic Oligonucleotide 131taatatgact tgacatcttc 2013220DNAArtificial SequenceSynthetic Oligonucleotide 132aactccaact gccgtactgt 2013320DNAArtificial SequenceSynthetic Oligonucleotide 133tctctcgagc ctcctgggta 2013420DNAArtificial SequenceSynthetic Oligonucleotide 134ccaaagtcag gccaggtggt 2013520DNAArtificial SequenceSynthetic Oligonucleotide 135gggactccaa agtcaggcca 2013620DNAArtificial SequenceSynthetic Oligonucleotide 136agggactcca aagtcaggcc 2013720DNAArtificial SequenceSynthetic Oligonucleotide 137cagggactcc aaagtcaggc 2013820DNAArtificial SequenceSynthetic Oligonucleotide 138tcagggactc caaagtcagg 2013920DNAArtificial SequenceSynthetic Oligonucleotide 139ggtgactcag ggactccaaa 2014020DNAArtificial SequenceSynthetic Oligonucleotide 140cctgactctc ggactttgaa 2014120DNAArtificial SequenceSynthetic Oligonucleotide 141gctgagtgag cctgactctc 2014220DNAArtificial SequenceSynthetic Oligonucleotide 142ccgtgctctg ggctgagtga 2014320DNAArtificial SequenceSynthetic Oligonucleotide 143aaggtccctg acctgccaat 2014420DNAArtificial SequenceSynthetic Oligonucleotide 144tctttcctct tgtccatcag

2014520DNAArtificial SequenceSynthetic Oligonucleotide 145gtctttcctc ttgtccatca 2014620DNAArtificial SequenceSynthetic Oligonucleotide 146ggtctttcct cttgtccatc 2014720DNAArtificial SequenceSynthetic Oligonucleotide 147gggtctttcc tcttgtccat 2014820DNAArtificial SequenceSynthetic Oligonucleotide 148aacagcactt tcttgatgtc 2014920DNAArtificial SequenceSynthetic Oligonucleotide 149ggaacctgcg catctccaac 2015020DNAArtificial SequenceSynthetic Oligonucleotide 150tggtcggccg tctggatgag 2015120DNAArtificial SequenceSynthetic Oligonucleotide 151gagaagcgca gttggtcggc 2015220DNAArtificial SequenceSynthetic Oligonucleotide 152aggtaggaga agcgcagttg 2015320DNAArtificial SequenceSynthetic Oligonucleotide 153gccaggtagg agaagcgcag 2015420DNAArtificial SequenceSynthetic Oligonucleotide 154agccaggtag gagaagcgca 2015520DNAArtificial SequenceSynthetic Oligonucleotide 155cagccaggta ggagaagcgc 2015620DNAArtificial SequenceSynthetic Oligonucleotide 156acagccaggt aggagaagcg 2015720DNAArtificial SequenceSynthetic Oligonucleotide 157cacagccagg taggagaagc 2015820DNAArtificial SequenceSynthetic Oligonucleotide 158tcacagccag gtaggagaag 2015920DNAArtificial SequenceSynthetic Oligonucleotide 159atcacagcca ggtaggagaa 2016020DNAArtificial SequenceSynthetic Oligonucleotide 160gatcacagcc aggtaggaga 2016120DNAArtificial SequenceSynthetic Oligonucleotide 161cgatcacagc caggtaggag 2016220DNAArtificial SequenceSynthetic Oligonucleotide 162tcgatcacag ccaggtagga 2016320DNAArtificial SequenceSynthetic Oligonucleotide 163caccctcgat cacagccagg 2016420DNAArtificial SequenceSynthetic Oligonucleotide 164tccttccact gatcctgcac 2016520DNAArtificial SequenceSynthetic Oligonucleotide 165ctccttccac tgatcctgca 2016620DNAArtificial SequenceSynthetic Oligonucleotide 166gctccttcca ctgatcctgc 2016720DNAArtificial SequenceSynthetic Oligonucleotide 167agctccttcc actgatcctg 2016820DNAArtificial SequenceSynthetic Oligonucleotide 168aagctccttc cactgatcct 2016920DNAArtificial SequenceSynthetic Oligonucleotide 169aaagctcctt ccactgatcc 2017020DNAArtificial SequenceSynthetic Oligonucleotide 170gaaagctcct tccactgatc 2017120DNAArtificial SequenceSynthetic Oligonucleotide 171ggaaagctcc ttccactgat 2017220DNAArtificial SequenceSynthetic Oligonucleotide 172gggaaagctc cttccactga 2017320DNAArtificial SequenceSynthetic Oligonucleotide 173tgggaaagct ccttccactg 2017420DNAArtificial SequenceSynthetic Oligonucleotide 174tggccgggga ggtgggggca 2017520DNAArtificial SequenceSynthetic Oligonucleotide 175tgggtggccg gggaggtggg 2017620DNAArtificial SequenceSynthetic Oligonucleotide 176tgcgtttggg tggccgggga 2017720DNAArtificial SequenceSynthetic Oligonucleotide 177tgcacttgcc attgtgaggc 2017820DNAArtificial SequenceSynthetic Oligonucleotide 178acttcagtgt cttgactcat 2017920DNAArtificial SequenceSynthetic Oligonucleotide 179aacttcagtg tcttgactca 2018020DNAArtificial SequenceSynthetic Oligonucleotide 180taacttcagt gtcttgactc 2018120DNAArtificial SequenceSynthetic Oligonucleotide 181ctaacttcag tgtcttgact 2018220DNAArtificial SequenceSynthetic Oligonucleotide 182gacagatgcc tgagcacttt 2018320DNAArtificial SequenceSynthetic Oligonucleotide 183gaccaggaag ggcttccagt 2018420DNAArtificial SequenceSynthetic Oligonucleotide 184tgaccaggaa gggcttccag 2018520DNAArtificial SequenceSynthetic Oligonucleotide 185ttgaccagga agggcttcca 2018620DNAArtificial SequenceSynthetic Oligonucleotide 186gttgaccagg aagggcttcc 2018720DNAArtificial SequenceSynthetic Oligonucleotide 187gcacacgttg accaggaagg 2018820DNAArtificial SequenceSynthetic Oligonucleotide 188gaggtacgcg ccagtcgcca 2018920DNAArtificial SequenceSynthetic Oligonucleotide 189tacccggtaa cagaggtacg 2019020DNAArtificial SequenceSynthetic Oligonucleotide 190agtgaaaaca tacccggtaa 2019120DNAArtificial SequenceSynthetic Oligonucleotide 191caaatcctaa cctgggcagt 2019220DNAArtificial SequenceSynthetic Oligonucleotide 192ttccagttcc accacaggct 2019320DNAArtificial SequenceSynthetic Oligonucleotide 193ccagtgcaca gatgcccctc 2019420DNAArtificial SequenceSynthetic Oligonucleotide 194acaggttaag gccctgagat 2019520DNAArtificial SequenceSynthetic Oligonucleotide 195gcctagcatc ttttgttttc 2019620DNAArtificial SequenceSynthetic Oligonucleotide 196aagccagcag gaactttaca 2019720DNAArtificial SequenceSynthetic Oligonucleotide 197gggacacctg agggaagcag 2019820DNAArtificial SequenceSynthetic Oligonucleotide 198ggtcatctgc aagatggcgg 2019920DNAArtificial SequenceSynthetic Oligonucleotide 199gccaacctct gatgaccctg 2020020DNAArtificial SequenceSynthetic Oligonucleotide 200tggaagcccc agctctaagc 2020120DNAArtificial SequenceSynthetic Oligonucleotide 201tagtaatgac tttccaatca 2020220DNAArtificial SequenceSynthetic Oligonucleotide 202tgagtcttgc tttacacctc 2020320DNAArtificial SequenceSynthetic Oligonucleotide 203cctgcgcgcg gagtgacttc 2020420DNAArtificial SequenceSynthetic Oligonucleotide 204aggacgtcac tgcagcagga 2020520DNAArtificial SequenceSynthetic Oligonucleotide 205tcaggacaag tcttggcagt 2020620DNAArtificial SequenceSynthetic Oligonucleotide 206gaggctgcac agtaagcgct 2020720DNAArtificial SequenceSynthetic Oligonucleotide 207tcagccaacc agcatcagag 2020820DNAArtificial SequenceSynthetic Oligonucleotide 208acccacagtg tccacctccc 2020920DNAArtificial SequenceSynthetic Oligonucleotide 209agtgcgggct gtgctgctgg 2021020DNAArtificial SequenceSynthetic Oligonucleotide 210cagctcgctc tggcggcctc 2021120DNAArtificial SequenceSynthetic Oligonucleotide 211aggaagggag ctgcacgtcc 2021220DNAArtificial SequenceSynthetic Oligonucleotide 212ccctcacgat tgctcgtggg 2021320DNAArtificial SequenceSynthetic Oligonucleotide 213cagtggagcg gctcctctgg 2021420DNAArtificial SequenceSynthetic Oligonucleotide 214caggctgaca ccttacacgg 2021520DNAArtificial SequenceSynthetic Oligonucleotide 215gtcctacctc aaccctagga 2021620DNAArtificial SequenceSynthetic Oligonucleotide 216ctgccccagc accagccaca 2021720DNAArtificial SequenceSynthetic Oligonucleotide 217attgcttcta agaccctcag 2021820DNAArtificial SequenceSynthetic Oligonucleotide 218ttacatgtca ccactgttgt 2021920DNAArtificial SequenceSynthetic Oligonucleotide 219tacacatgtc atcagtagcc 2022020DNAArtificial SequenceSynthetic Oligonucleotide 220ttttctaact cacagggaaa 2022120DNAArtificial SequenceSynthetic Oligonucleotide 221gtgcccgcca gtgagcaggc 2022220DNAArtificial SequenceSynthetic Oligonucleotide 222cggcctcggc actggacagc 2022320DNAArtificial SequenceSynthetic Oligonucleotide 223gtggaatgtc tgagatccag 2022420DNAArtificial SequenceSynthetic Oligonucleotide 224agggcgggcc tgcttgccca 2022520DNAArtificial SequenceSynthetic Oligonucleotide 225cggtcctggc ctgctccaga 2022620DNAArtificial SequenceSynthetic Oligonucleotide 226tacactgttc ccaggagggt 2022720DNAArtificial SequenceSynthetic Oligonucleotide 227tggtgccagc agcgctagca 2022820DNAArtificial SequenceSynthetic Oligonucleotide 228cagtctcttc agcctcaaga 2022920DNAArtificial SequenceSynthetic Oligonucleotide 229aagagtcatg agcaccatca 2023020DNAArtificial SequenceSynthetic Oligonucleotide 230tgaaggtcaa gttcccctca 2023120DNAArtificial SequenceSynthetic Oligonucleotide 231ctggcaagag gcagactgga 2023220DNAArtificial SequenceSynthetic Oligonucleotide 232ggctctgtgc tggcttctct 2023320DNAArtificial SequenceSynthetic Oligonucleotide 233gccatctcct cagcctgtgc 2023420DNAArtificial SequenceSynthetic Oligonucleotide 234agcgcctgct ctgaggcccc 2023520DNAArtificial SequenceSynthetic Oligonucleotide 235tgctgagtaa gtattgactt 2023620DNAArtificial SequenceSynthetic Oligonucleotide 236ctatggccat ttagagagag 2023720DNAArtificial SequenceSynthetic Oligonucleotide 237tggtttattc tatggccatt 2023820DNAArtificial SequenceSynthetic Oligonucleotide 238cgctcctgca aaggtgctat 2023920DNAArtificial SequenceSynthetic Oligonucleotide 239gttggaaacg gtgcagtcgg 2024020DNAArtificial SequenceSynthetic Oligonucleotide 240atttattgtt gcaactaatg 202412346DNAMus musculusCDS(710)...(2008) 241gaattcggga tccttttgca cattcctagt tagcagtgca tactcatcag actggagatg 60tttaatgaca tcagggaacc aaacggacaa cccatagtac ccgaagacag ggtgaaccag 120acaatcgtaa gcttgatggt gttttccctg actgggtagt tgaagcatct catgaatgtc 180agccaaattc cgtacagttc ggtgcggatc cgaacgaaac acctcctgta ccaggttccc 240gtgtcgctct caatttcaat cagctcatct atttgtttgg gagtcttgat tttatttacc 300gtgaagacct tctctggctg gccccgggct ctcatgttgg tgtcatgaat taacttcaga 360atcatccagg cttcatcatg ttttcccacc tccagcaaga accgagggct ttctggcatg 420aaggtgagag ccaccacaga ggagacgcat gggagcgcac agacgatgac gaagacgcgc 480cacgtgtgga actggtaggc tgaacccatg ctgaagctcc acccgtagtg gggaatgatg 540gcccaggcat ggcggaggct agatgccgcc aatcatccag aacatgcaga agccgctgct 600ggggagcttg gggctgcggt ggtggcgggt gacgggcttc gggacgcgga gcgacgcggc 660ctagcgcggc ggacggccgt gggaactcgg gcagccgacc cgtcccgcc atg gag atg 718 Met Glu Met 1gag aag gag ttc gag gag atc gac aag gct ggg aac tgg gcg gct att 766Glu Lys Glu Phe Glu Glu Ile Asp Lys Ala Gly Asn Trp Ala Ala Ile 5 10 15tac cag gac att cga cat gaa gcc agc gac ttc cca tgc aaa gtc gcg 814Tyr Gln Asp Ile Arg His Glu Ala Ser Asp Phe Pro Cys Lys Val Ala 20 25 30 35aag ctt cct aag aac aaa aac cgg aac agg tac cga gat gtc agc cct 862Lys Leu Pro Lys Asn Lys Asn Arg Asn Arg Tyr Arg Asp Val Ser Pro 40 45 50ttt gac cac agt cgg att aaa ttg cac cag gaa gat aat gac tat atc 910Phe Asp His Ser Arg Ile Lys Leu His Gln Glu Asp Asn Asp Tyr Ile 55 60 65aat gcc agc ttg ata aaa atg gaa gaa gcc cag agg agc tat att ctc 958Asn Ala Ser Leu Ile Lys Met Glu Glu Ala Gln Arg Ser Tyr Ile Leu 70 75 80acc cag ggc cct tta cca aac aca tgt ggg cac ttc tgg gag atg gtg 1006Thr Gln Gly Pro Leu Pro Asn Thr Cys Gly His Phe Trp Glu Met Val 85 90 95tgg gag cag aag agc agg ggc gtg gtc atg ctc aac cgc atc atg gag 1054Trp Glu Gln Lys Ser Arg Gly Val Val Met Leu Asn Arg Ile Met Glu100 105 110 115aaa ggc tcg tta aaa tgt gcc cag tat tgg cca cag caa gaa gaa aag 1102Lys Gly Ser Leu Lys Cys Ala Gln Tyr Trp Pro Gln Gln Glu Glu Lys 120 125 130gag atg gtc ttt gat gac aca ggt ttg aag ttg aca cta atc tct gaa 1150Glu Met Val Phe Asp Asp Thr Gly Leu Lys Leu Thr Leu Ile Ser Glu 135 140 145gat gtc aag tca tat tac aca gta cga cag ttg gag ttg gaa aac ctg 1198Asp Val Lys Ser Tyr Tyr Thr Val Arg Gln Leu Glu Leu Glu Asn Leu 150 155 160act acc aag gag act cga gag atc ctg cat ttc cac tac acc aca tgg 1246Thr Thr Lys Glu Thr Arg Glu Ile Leu His Phe His Tyr Thr Thr Trp 165 170 175cct gac ttt gga gtc ccc gag tca ccg gct tct ttc ctc aat ttc ctt 1294Pro Asp Phe Gly Val Pro Glu Ser Pro Ala Ser Phe Leu Asn Phe Leu180 185 190 195ttc aaa gtc cga gag tca ggc tca ctc agc ctg gag cat ggc ccc att 1342Phe Lys Val Arg Glu Ser Gly Ser Leu Ser Leu Glu His Gly Pro Ile 200 205 210gtg gtc cac tgc agc gcc ggc atc ggg agg tca ggg acc ttc tgt ctg 1390Val Val His Cys Ser Ala Gly Ile Gly Arg Ser Gly Thr Phe Cys Leu 215 220 225gct gac acc tgc ctc tta ctg atg gac aag agg aaa gac cca tct tcc 1438Ala Asp Thr Cys Leu Leu Leu Met Asp Lys Arg Lys Asp Pro Ser Ser 230 235 240gtg gac atc aag aaa gta ctg ctg gag atg cgc agg ttc cgc atg ggg 1486Val Asp Ile Lys Lys Val Leu Leu Glu Met Arg Arg Phe Arg Met Gly 245 250 255ctc atc cag act gcc gac cag ctg cgc ttc tcc tac ctg gct gtc atc 1534Leu Ile Gln Thr Ala Asp Gln Leu Arg Phe Ser Tyr Leu Ala Val Ile260 265 270 275gag ggc gcc aag

ttc atc atg ggc gac tcg tca gtg cag gat cag tgg 1582Glu Gly Ala Lys Phe Ile Met Gly Asp Ser Ser Val Gln Asp Gln Trp 280 285 290aag gag ctc tcc cgg gag gat cta gac ctt cca ccc gag cac gtg ccc 1630Lys Glu Leu Ser Arg Glu Asp Leu Asp Leu Pro Pro Glu His Val Pro 295 300 305cca cct ccc cgg cca ccc aaa cgc aca ctg gag cct cac aac ggg aag 1678Pro Pro Pro Arg Pro Pro Lys Arg Thr Leu Glu Pro His Asn Gly Lys 310 315 320tgc aag gag ctc ttc tcc agc cac cag tgg gtg agc gag gag acc tgt 1726Cys Lys Glu Leu Phe Ser Ser His Gln Trp Val Ser Glu Glu Thr Cys 325 330 335ggg gat gaa gac agc ctg gcc aga gag gaa ggc aga gcc cag tca agt 1774Gly Asp Glu Asp Ser Leu Ala Arg Glu Glu Gly Arg Ala Gln Ser Ser340 345 350 355gcc atg cac agc gtg agc agc atg agt cca gac act gaa gtt agg aga 1822Ala Met His Ser Val Ser Ser Met Ser Pro Asp Thr Glu Val Arg Arg 360 365 370cgg atg gtg ggt gga ggt ctt caa agt gct cag gcg tct gtc ccc acc 1870Arg Met Val Gly Gly Gly Leu Gln Ser Ala Gln Ala Ser Val Pro Thr 375 380 385gag gaa gag ctg tcc tcc act gag gag gaa cac aag gca cat tgg cca 1918Glu Glu Glu Leu Ser Ser Thr Glu Glu Glu His Lys Ala His Trp Pro 390 395 400agt cac tgg aag ccc ttc ctg gtc aat gtg tgc atg gcc acg ctc ctg 1966Ser His Trp Lys Pro Phe Leu Val Asn Val Cys Met Ala Thr Leu Leu 405 410 415gcc acc ggc gcg tac ttg tgc tac cgg gtg tgt ttt cac tga 2008Ala Thr Gly Ala Tyr Leu Cys Tyr Arg Val Cys Phe His420 425 430cagactggga ggcactgcca ctgcccagct taggatgcgg tctgcggcgt ctgacctggt 2068gtagagggaa caacaactcg caagcctgct ctggaactgg aagggcctgc cccaggaggg 2128tattagtgca ctgggctttg aaggagcccc tggtcccacg aacagagtct aatctcaggg 2188ccttaacctg ttcaggagaa gtagaggaaa tgccaaatac tcttcttgct ctcacctcac 2248tcctcccctt tctctgattc atttgttttt ggaaaaaaaa aaaaaaagaa ttacaacaca 2308ttgttgtttt taacatttat aaaggcaggc ccgaattc 234624220DNAArtificial Sequencemisc_feature(1)..(20)n = a, t, c, or g 242nnnnnnnnnn nnnnnnnnnn 2024375899DNAHomo sapiens 243gatcttcctg cctcagcctc cccagcagct gggccccacc acaccggcta attttttaac 60ttttagtagt gacgaggtct gattctgtta cccaggctgg tctggaactc ctggcctcaa 120gacatccgcc tgcctctgcc tcccaaagtg ctgggattac agatgtaagc caccgcgcct 180gggctcctat gatttttatt taacataatg caccatggaa tttgtgctct gcttagttca 240gtctgagcag gagttccttg atacttcggg aaacactgaa aatcattcca tccccatcca 300ttcattcctg cagcacccaa gtggaaattc tgcgtttcag acagggacac tacccttaga 360gagcagtggg cttccccagc agcgtagtga aacatgatac tcctgagttt catgaaaaaa 420gggcagacat ctggccagag ctgggaggca ggaaatagag cacggtgccc tcctcccata 480ctccagcttg gattactgag gctggggccc aggccctgca ggaaaggagg tgcatgacta 540ctttaaggcc actcactctg tgactcaacg ggccgggtcg gggctggaac tcaatgccct 600cccgggcctg gagagcccac gcgccgtggg cggggctccc ggggtcgcct aggcaacagg 660cgcgcgccgc gcccgagccc agagccccaa agcggaggag ggaacgcgcg ctattagata 720tctcgcggtg ctggggccac ttcccctagc accgcccccg gctcctcccc gcggaagtgc 780ttgtcgaaat tctcgatcgc tgattggtcc ttctgcttca ggggcggagc ccctggcagg 840cgtgatgcgt agttccggct gccggttgac atgaagaagc agcagcggct agggcggcgg 900tagctgcagg ggtcggggat tgcagcgggc ctcggggcta agagcgcgac gcggcctaga 960gcggcagacg gcgcagtggg ccgagaagga ggcgcagcag ccgccctggc ccgtcatgga 1020gatggaaaag gagttcgagc agatcgacaa gtccgggagc tgggcggcca tttaccaggt 1080gcgggagcgc cccggagcgt ggcgggccct tcgcttaggc cgcttgaaca tcccctcaga 1140cctccaggcc ccagactccc tctgggtctt gccctctgcc tcgctcctac tgcttgagga 1200ttcgatggga cagcgacgca ctgcgtcccc ccaccctttg tccccggggc gggcgtgttt 1260ctcgccgcag cgtcggagcc cccttcgatc ccccacctcc cttctgttct ccagctcggg 1320tgatctctca agccggggga ccgccggtct gtgctctcaa cgcgaatccc tcgcaccccg 1380accccgcccc ctgcctgtcc actctttgtc ccctggggtg atttagcacc cccactattt 1440ccttttctgg agtggaccac ctcagactct cttcctttgt ctccctgggg gaaaaggtta 1500ctccccccgt ccctccttca catttccttt cccctagtct cagtgtgcgt cgagtcccag 1560agatgacagt cccctttccc ctttctgttc attcatttat tggataggag ttggcaagct 1620tattctgtgc taggcaccgc ttaggcattg gaggtggtgt ttgctaatca ggacaggcaa 1680gatcctagcc ttagtggggc ctagagtcga atagggcaat caaacacaaa agcaaataat 1740ttcagatagt gacaggtgct gtgaagagaa cgacttccta acggggtaca gggtgactgc 1800atagaaggcc ggctgtctta gagaagggga tcagggaagg cctgtcaaag gaggagacat 1860ttgctttgtg agctgaacca agaggagcag aaagccgtga gaatatgggg ctaaagaacc 1920ttctagccag gaggcctgcg gtacccactc cattggggcc atgatattat tctttcaggc 1980agggactcag gaaggttaac gttttaaccc tctctaaaat agcatctttc ctcaatgagc 2040agcttagtct ttggtcgtgg cagagatgac cttgtcttag gagtcatctc cttgtgtgtt 2100aaaaagttag gaaaggaggg tttctcatat atctataaaa caagtagtta aaaacacaaa 2160gagctcttcc tttcacaagc agctgaataa gatacatact cccaattaaa tgtcattgcg 2220ggggttgtta agattaacta aaaccacact tgcacagtat cttaaataag cgatatacag 2280aatagagaga ttttgttact tgtgtaaagg gagacagcag atgattctgt tttcagctta 2340taggctcaaa aggcaaattg tgagatccat cagctgtagt attaaaatct attttgagct 2400ccgcttagaa aggaaaaaag gtttaagcag ttctttggta tgcttgacta acaaaagcct 2460ttttttttgg cagccttgat tttcatgtgg atttacatca agcttatttg acaggattct 2520ttttatttgg actgtagtgt gtatattagt ttctgctaga ctaatatttc taaccactgt 2580aatctatata ctaataagta tgattgatca gtatataaaa tttgtatgcc atatctggtc 2640tctgaattag ctgaatgaat tccataaggg actttgagac tgtgtagaca aattttctgc 2700atcagtttaa tgcagtagag tctaaaatgt ctttaaatga aaattgttgg tctgaagtgt 2760tggagttgat tatgatacac cccatcacag tggaagcatt gtggagagaa gtcttttcca 2820ctgaaattga ctgagttgac aacaagaaat acgtattgta acttagttct tagttgaatt 2880ttatttctta caattttaag ccagagtggg ttgacctgtc acccaagcat ggttaaaatt 2940gtattcagca tgcaactagc atggagtgtg tcagtcttca attcatttcc ttcattgttc 3000ttaagttttt ctgccacaat taaaccccac aagttagtca aggtgttgag attttcactg 3060cttcttaatg gattgccaca ttccctgagg tagtttcttt tggtcttaga gaattgtcag 3120ggccagcttt tctcacctcc actgtatgga tatttttctt ttctaagatc ttgaaatcag 3180aagcttttct cctaagtgta aaagtagctc tttgtcatac aactgtagcg ttttctgaaa 3240cagagttcag atgaccttga gtctaaagtg gctaactttc caaggtgtgt atcgctttac 3300caaaaccatt atttttcaag gattcaaaga atgtgtttac aattgataga aaatggaagt 3360ttaaaaaaat taatacttta tagcatgttg aaatgagggc agccttatac aaagtcatac 3420tttgagcttg cctagcctat tgtgatcaga gaataatgta atttttgctt acaacttggt 3480aagcaggtca gttattctaa cttattttct gattagaaca aaaagatgta aaaacttgaa 3540aactattggg aaaagaacaa agagtgaaga ggacttttga gtgctgagga atgtggcagc 3600ttggaaaaca aactttttag gcagagattc tttgctaggt cagtttgata aagtgagcat 3660aaccgtattt ttaatcttta atgctaatga atagcataga tgctaataag catctaggtc 3720tataaaaagt cagctttgat agtgtatata gatggcttta aacattgttt tctagcattt 3780aaacactttc aaatcatccg gttgcttgat tgggcctagc tgtctaagag gagagaatga 3840gcccagatga ggaaaagaga ttgattttac tgagctagaa tgagaggaga gagggttgag 3900tgaatgaaaa gaatagctca tgtgctcccc tccatctgta gtttaagagg ggttgggtcc 3960ggtgttttgc ttgttttctc gtctgtaaat tctttgattc tctgacacca ctcactatat 4020ttcattgtga atgatttgat tgtttcagat aaaggggact gcaataatac cttgtgacat 4080gaaggcaaga tttattcatg ttagaggcag gctttgtaaa atgggccact cttccaattg 4140acatttgttt ttatagctgt tttcattatg aaatacaatc taatgcctga ctaggttaaa 4200accatgttgt aacaatagtt cactaaaatt ccttactgat atacagctta tgttgttata 4260ttccaaaaag atgaatatta aaatttgcca ataatgttta tttaaatact attttcttca 4320gaggaaaaaa aactatttta tgcaaaggag aaagatctat acactatgac tcacttcact 4380taaaaaaaaa aagactaacg gaaatgacat ggagagactg ggaagttcta gtcatcttga 4440gtgacccatt agatctaaat gttcttgttt agccctggtt tgagtgaact aaatttaggt 4500gtctgatcag tactttggaa atggtgtaaa tgcctttgta attgtctgga ctgatattag 4560attaactggg agcacaagta gaaatagtga aggaaagaac tttttgctat tgttatttga 4620catcactggc atatttatag gaatactttg gtgtttttgg aagtaagtaa accaaccagt 4680ggttctaaaa agtcagctgg gggataatgg taatgccgct gtttcttagc tgcaagttat 4740ctgccgttac ttctcctcca ttttgcattt tatcttgaat agctcctcaa aacctattaa 4800aatacctggt attgaataat gtaattgaat gtgtactgaa tttcacagtg gaaatgaata 4860agaaatttcc tgtggaggtt ttttgactta gctactgaaa taacggcctt ttgttgtgtg 4920attctttccc ttttctcttt gttaaagaaa actgtcttgt gatcttgtag attacagaat 4980ccttttggca atttctgttc ctagcactgc tttttctttc tttctttctt ttaaatagaa 5040atggggtttt gctgtgttgc ccaggttggt cttgaactcc tggcttcaag cgatcctccc 5100accttggcct cctgaagttg ggattgcagg cgtgagcagg tactttttct gaggcctgcc 5160tgagcctata tatattttgc acaatttggc attcctccct acagtgttta tgctgatttg 5220tttctggtaa caactaatac tggcaaatcg gctgggcatg ttactttatg ctgcccatat 5280tcaggaaaat tggaattcta gctgggtcat tgttcccaga tgatgtagtt tggcaccagc 5340cattccatgt tcacattttg agtatccagg agggctgggg actttggagt agttggtgat 5400tccctctgcc acatttcact ggttggtcac tatggcatcc tttccaccac actagtagtc 5460taggttctca gatgttgctt atgagcctgc aatggtttct agtttcacac tgcagaaatg 5520agtgaagccg gttacccgtt aatatggtcc catcatcact agagtaattc attgttctaa 5580aaccagatct gagtctctca ctcctctgca actacttctg attctttcat aacacttgta 5640aagtccaaac tcctctttag catggcagcc agcttccagt ccttccctcc tatgtggctt 5700ccattctagc cagacaagaa agggcagcgt tctccaaact catcctcgcc cttcattcct 5760ctataccatt gctgagcact ttgttgagga tgcctctccc gttcaatcta gcttgcatct 5820tccagctcga atgtgtgctt ccttgcacca gagttttgtt ccgtcacctg tgtgttttca 5880tacaagctgg cacatatctc ttctaaagcc ctgctgtcat tgtagctgcg tctttacaaa 5940catttttttt ttaaattttt ataaagtcaa ggtctcacta tattgcccag gctggtctca 6000aactcctggg ctcaagtgat cctcctgcct tggcctccca gagtgctggg attataggta 6060tgagacactg tgcccagctg tagctgctac tttatatccc aggtctatct ccaatggagc 6120ccaagcttcc tgaggccacc tgttgtatct ttctcattca tcttgaagtc ctctgctcct 6180ggcacagagt aggtacctaa caagagttgg gattgaattg atggtcagta ctttgctagc 6240ctgatggtat aaagatgtac aaaacatgtt cctggctccc actctagggg ggcaatgatg 6300gaaacaaata gattagccca cattagtacc aatagtagag gtcactctgg gagaaggccc 6360ccaccacatt ttgagtcatg gcctaatgag gtaatttagt attgcctgct gcagtggctt 6420tggaagaaag gctggcattc ttagccagta gaagctgata ccactgattt gtttcacaga 6480agctttaaat ataacaataa atttgtgctt ggcctacggt gaactttaca ggcaacttgg 6540aggtaatatg tttgtctctc taagaattgt tgaattcctc ttccctcatc cctcctgact 6600ggttctcaca agcctagcgg gcctttgcat gtggttggtt cataaaatac tttttgattt 6660tgggatataa aatatagttc tccataaaat aacgactgtt accaagtctt tgattttttt 6720tttcaaacta taaatggtaa tgacattctt tggcctttga tcagaccacc cttaggggca 6780agagagtagt ttcatgtttt gctttttcta gtgtcccctg tgtctgggta tagttgcagt 6840ctcagctgtc atactaacag tgctgagtga gtcccttact ttctttgggt tttggtttct 6900cccttgtaaa aatgatcctg gactaactga tcattaagtt caggtcaagt aataaaaatc 6960cttaatgtac tcacaaatac aatttaatgt tcctgaataa tccttgtaaa aactgcagca 7020gttactcagt tttgtaaggt gtggttgggt actattaggc tcaaaagttt ataggagctt 7080tgtgagtata gttaacaact caaaagaatg gggtgttttt tcccgagggg catgaaatgt 7140ttttgataaa tagagttcat ttgacttggt aatgtggaaa atgagtagcc ctgacacgta 7200cgctatgctt ttgcagtttt tctctcaagt agcaattggg tggcttttcc tgtaaaagat 7260agaggaactg attcttgaga atttacgaaa gcttcaaccc taactaggta tgcaaagaat 7320agttgccctt tatgttgtaa ttttaggaag aaacctacat ctggtctaag tttcatttga 7380ataatatgat agtttacaca tctgccatat ttgagaagaa agtacctaag tctccagcat 7440tttagaaata atgctttact ttgtgtagaa atggtcttta gagtttaata gctgctgccc 7500tctccttttt caaagcagct tgacataatc atgagtatct tgctgacagc ttgtaaattt 7560tgattgtatg aaaactgaaa ataagaccat ttcacatgga agattccctc ctgccctgaa 7620acagccaaag aaaactgtag ccatcaaatc tattgatctc tgggctttgg tacaagtcac 7680actactacaa ataaaataat accaagtact tataaatgat tttcagtcct tttaaagttt 7740atttttttaa tatttttttt gagatggggt cttgctgtgt cgtccaggct ggagtgcagt 7800ggcacaatct tggctcactg caacctccac ctcctgggct caagtgatcc tcccacctca 7860ggctcccaag tagctgagac tacaggcatg tgccatcacg cccagctaat ttttgtattt 7920ttttggagta gagatgggat tttgctgtgt tgcccaggct ggtcttgaac tcctgggctt 7980aagccatctg tctgcctcag gctcccaaag tgttgggatt acaggtgtga gccactgtgc 8040ccggcccagc ccttttttta agagaaaaac gtatgacatc gttcgattta ctgagtgctt 8100atggttttac taaggcagta aggttttatg gataccctat ggtaattaga tagaattagt 8160gctctgaagt cagctctgta atatggactc agagtaaaca tggcaaaggg acacttaagg 8220tctgcatttt ctctgggaaa taaacgtatt ctttactact ctgaatctag tgctgggaaa 8280ttctaaatcc ttcttgagga ttaaccactt gaagtaaagt tttgggtccc aagtaggctt 8340gtgtccctgt ctccttctct ttacttttca gatgtttctt cctagagact gaggtatatt 8400ttacttttac agatgaagaa ggaagcctcg gctgtgtttg tggcttttgt gggtgagcaa 8460catcacttgc aaagataaga tgagcatagc aaaactaggc tttcaaaata atttttaaaa 8520atttcttagt gattagaaaa ggaaaactct tcccttgtct ctgttaagaa acgtttttcg 8580acttttttcc tttcttaatg gatcttttat tggcacttct cttccttttg cagaatctta 8640cttaaaagtc actacgttac attacagcaa acagcttagc taatttttat ccagatgggc 8700cccggttaca ggattgtaca ctattgcgaa tttcttacag gaaagtgaac atcaagtaat 8760tattccaaat agagttctct taagaacgtg agttacttaa aaatgtctaa ggatgaagtc 8820acttctgaat ataacttcac tcaagagaac aaataagcaa actgcattta gcataacatg 8880gtaaattagc tttaactctc cttgatgttt gaacatttgt cgctgttaac tactgtttca 8940cttttcaaat agtcagggct tagtttgctt ctgtaaggat aaagggaaaa tacgccttca 9000ctgagtcata aatatttttg tggctaactt ttgcacagag aaaagaggcc tctaagaagg 9060tacccagtga attttttttt cggggcaggg agagaatatg tcattttttg gtttgttgtt 9120gttgttgtca ttgttttgct ttgttgtttt tactctgaac tgaactgtat cttgacagca 9180cttttgaatt aagagcatta ctcttattgt tctctactac ctggacgcca cctccctgtt 9240gccatagtgt taaggatcat gctccgaggt ggggtgaggc agaatggggc caagatcaga 9300aagttacatt aagctacatc aggtttatac aagcataaaa ccaaattttt ggagcagtcc 9360ccagaataca acctggttta gccacaccta aaggttgctc ttgaatattc cttgagaatc 9420cacatcccta gaatgctggg tttcaatggg ccctttatgt acctatcatg gtgtcatttc 9480tgagcatttc taaatattcc ttcatgtctt actgacagtt tttcttgaat aaatcttagg 9540aatattagtg ccattatcag tattttgttt ggtctgttca caccacaaat aactacccag 9600gtctgctact tgcccctatt tctctacctg ctaatgaaaa tgcttttgaa agtttgagta 9660acagtattgg agtgtgcaca gtggtattgg taggttctgt actcatcctt aaccacttgt 9720tttcatcctt tgtgagcttg aagtttctcc aaaaaattta tcacaaaact tatcagacat 9780agttaataca ctcagagaga gaatcactga aaaagtagat gtagtttaac aaacccagtg 9840cctttttttt acccatgaat acatatttgt caactaaacc tcattttgca acttgttcca 9900ctactcgaat ggtaacaaac ttttggtttc ccaatagatt tggaagatgt tgcttttgaa 9960agtaggaaat agatggcttt agaagatgga agaatatttt gtttgaagtg ggagcgtggt 10020atgtccttag ctgtctgtga aatgcagctg aagatgggtg tgggccttca tctgcatttc 10080ccatcttcag tttgaggagg tagttaccct tctaaccact taagaactgc atggtacatg 10140ctgttttatt tacagggcaa aactgtgctc ccgtagtttc cctggtgctt gccttcacgt 10200taacacagtg tcatcgtttg gcagtgttta tgtgccaggg tccatgttag aaggaggaaa 10260ggtatagcga agttaaaggg tgcagttggc ctcccacctt tagttttgta agtgccttta 10320aagtttgatt tttgtaggtt gatcataagg aagtgataag tatgttaggt tatttgtggt 10380ttgagctaat tttagtctct ttttacagct tgctttgtat cctttgccat taaaacatgc 10440tttctagaaa gacaactttt gaatgtagga cacagtctat attctatact tggctacatt 10500tcaaaaaata ttttctcagt actttggaag ttggacagtt ggaagcatag tgacagtatt 10560taaaaatctt tgattccggc cgggcatggt ggctcacgcc tgtaatccca gcactttggg 10620aggccgaggt gggtggatca cttgaggtcc ggagttcagg accagcctga ccaacatggt 10680gaaaccctgt ctctactaaa aatacaaaat tagccgagcg tggtggtaca tgcctgtaat 10740cccagctact caggaggctg aggcaggaga atcgcttgaa tctgggaggc ggaggttgca 10800ttgagccgag atcataccat tgcactacag cctgggggac aagagtgaaa ctctgtctca 10860aaaaaaaaaa aaaaattaag tgatttcttt gctttgtgac acttctactt ttccagcaag 10920taaattatat tctttcatac aggtatgaaa ttcttgttcc aagctagtgg ttaaaaaggc 10980acagttgata ttagaggatt tgtaaaagat tatgaccacg cctgcaatgt actgaagcaa 11040ggctttgctg ggctgtgtat aggaaacctt ccccagcctg tgcccttgct tgatagaaca 11100ttttgctcct aagggtaggt gcctgtatct gtctccagta ctggttagtt tcacacagaa 11160cagttgtgtt tcagagcttt agtctcaagc tgccctgctc ccctgaagca gccaccctga 11220gcatgtgcac tcacaggagg ggacatgtga ggtcatggaa gaagacgact caggaagaag 11280aagacttggg tttgggttct gactctgcct ttgactgttg tgggattttg aggagttgca 11340tacaggatct gtaaaatgta gtcattagac tagactagac agccatatag cattacctag 11400atgtaacttt ctacaaagac atggtcacag gagaagacca gagggtgggg tgatctttct 11460ggaaaaattg gggcttcatg ccttactcat gctagatatg gtagcattat atggctgtgc 11520ctgatccccc taatctaaaa gtgggacaga actttaaaat ttcatattaa ctcaaattaa 11580aacttgaaaa aaacccatta tttccttaaa aataataaaa tgccctgtgg gggcataagt 11640cacattatat tttaaaattc ctgaatgcca catggatgaa tgtagttcct tttgaaattc 11700ttcttttgtc taaagaggaa tgttggattt tgtaattgga ctaaaaaatc ttccatttga 11760gagagaaaca gtctgctgca tgttctaccc ttgttcagga taaaacccac taatagctaa 11820catttattga attctgtgtt gtgcctcagg cactgtgcaa agtcctttac atgcaatgct 11880gtttattata tactgtcaat tggtctataa cagcaggaaa tgtttcagga ggacaatgag 11940gtcccagacc ctcagtcttc tcctgtgtcc tggattcagc ttcacaatag cactatggca 12000gtgtggccac tgcttcagct tccacataca tggctgtgaa gagagacagg ggattgtgct 12060aagcctcccc gatttattag gacataggag gagagagttt gtagtttttg acctttgcct 12120agttttctaa cctctttcct agatgtcaca aattggccac ccacagtcat attttgcttg 12180cttcacgcaa tgctttttaa aaaagagaag agtttaattt gtgccattgt ttataaatga 12240atcaggagaa atgacatgca actctggatt ctggcctctc ttgaaaaatc tgaaaatcac 12300accgtctgag cttacactgg cagtggtctg ctggactgag ggacacaact ccttttggat 12360gtacatgtgt gcgttgcaga gtttaccaca gtcccacagt gggtcacact gtccttgtcg 12420gtgtacacta cctagcactt gagtttgcaa cccctacccc aagctgagtt ttctcgtcaa 12480gcttgatgtt aatgttatgt gatgcttggc cttgtaggta tttggtatat tatcgttaga 12540taaaattgaa gcaaagggct aaagggttgg tggcctgagg gagtgccctt gacagtaaag 12600tctaggataa aatcattggc caggtactcc ttcccttccc gcccttcctc ttttctcttt 12660atcctcagcc tccttctgct attttgagga agttagaagc caccaccatt ttttcccacc 12720tcaggcaact gagtgtggct gtatttctgt cccatgttca gttatttcca ggaactattt 12780ttgatgacca acttgaagtt acattgggtg ggcctaatgg gggctgataa aagaatgagg 12840tgaccaaata tgcttgcact gagacggcta cgaagtaagg tttttaatga cttgctttgt 12900gacttggtca ggagtgatac catttgtcat gtgtccaact tcatgactaa atggttgctc 12960taccttatcc tcatagctat aataaaataa aataaataca tacattgcag ggaggaatgt

13020atcttgttaa aggtctctcc cttttagcaa caaaagtaca tattatgttg tagaacatgc 13080tttttctttg atccttcttg aacacctatt actctataga ggtatgttgt gtatggcaaa 13140ttagaacaag caatagataa ggatgattct ttaccattat aacccagtca aggtctttgt 13200cctaagtttt gtacctttct ccagagggaa aggtatttgt atttatttat ttatttttga 13260ggcagagttt tgctcttgtt gcccaggctg gggtgcaatg gcacgatctc agctcactgt 13320aacatccgcc tcccgagttc aagtgattct cctgcctcag cctcccgagt agctgggatt 13380acaggtgcct gccacgatgc ccggctaatt tttttttttt tttttgtatt tttagtagag 13440atggggtttc atcatgttgg ccaggctggt cttgaactcc tgacctcagg tgatccatcc 13500acctcggcct cccaaagtgt tgggattaca ggcatcagcc actgcctccg gccaggtatt 13560tgtattttta gtctctatgc cttaccgtct cagatcagga ggatttggtg atttatcgaa 13620tgtgggggaa ggggaagaag aggaaacggg aggaatgttc cagattaggg aaatagctag 13680atggaagatg cagcccctca tcaaggtggg gacacaggaa aaggaacgtg tgcaaagaag 13740atggtgatct ggttgtgacc atgttgttag aggacgtcca gggaagcatc tggtaggtgg 13800tggggtgttt aaatatagaa cattcggaga atgctccgaa gcttcagaga acccttccca 13860aaaggacaaa accagctcag tgttttagca ctccgggatc atatggcatg acagcatggc 13920tgctttatac ttttttgtgt atgtgaaatt aaaaccaacc actcaggacc aatttctctg 13980aagctttttg tcaatctttc atttgctttt ctcgtctaga ttgtaagctc cttgcagcca 14040gtgtctgttg attcagtcat tcaaaaaata atacatgaac agctactagg taccaggctc 14100tgtgctgggc agttgggata tgtggtgagg aagacaaact tggtccctgc ccttaggaag 14160ttcagtagtc cagcagacaa agtggctgaa taaagataat ctcagttcac agtgataaga 14220gctcttacag gcctaggctc caggtgctgt ggggatgctc aggaaaaggt atctaattgg 14280gattgggagc aggcaaaaca aataaaggat agtgtataaa ggtaatatct agttgaagtt 14340ctgaagggca aggaggagtg agcctgtata ttctctgagt ctctccctaa tctgggattg 14400acttcttgtc cgtctctgtt catattaagt gtcacctagg cttgaaaggg tgagatcata 14460tttcacttcc ttcctctttg gtcttaacct ttctctgcta ccccctcaca caatgcatat 14520gcattattct cttattgtat atatttttcc tctcttcctt ttcatgtttc ctctgccatt 14580acttttaacc tcgactgcca tatggcctct aaacgcttcc agaagggtag cctagtggag 14640gttattccat catggccttg agctcatgcg accagatagt gaaggcatct gtgtaggtgt 14700cttctccagg agggtgatat ttgtttcatt gtaaattttg tagccctaga acaccaacaa 14760cagtgcacag taattagtag gcaggcagta caggattcat tgaagtgaag tgataacttt 14820tatccaagta tgtatgcaga taatctttga tttgtacaaa aaaaattata ttttaatatg 14880taaagatttt ttaaaagaat cttcaagttt tagccttccc actaggaata tattgaaaac 14940atgtgcctag ttcactgact tgcagctgcc actatgagaa taaaggtctc atttagttgt 15000tgtgaatttt aagggatatt ttcaatgatg ttggctggtt tatcccatta tgtggtcttt 15060tttttttttt tttttttttt ttgaggtgga gtctcgctct gtcacccagg ctggagtgca 15120gtggcgcaat ctcgactcac tgcaacctcc gcctcccggg ttcaagcgat tctgctgtct 15180cagcctccta agtagctggg attacaggcg cctgccacta cgcccagcta atttttggta 15240tttttggtag agaagggttt caccatgttg gtcaggctgg tctcgaactc ctgacctcat 15300gatccactca cttcagcctc ccaaagtgct gggattacag gcgtgagcca ccatgcccag 15360cctatgtgct cttattagca attctcagta cacagatagc tttgagtgat tctttcaagt 15420caagtacctt attaaaaaac tcaagtgtac tgataattat cttactttta aatggctaag 15480tgataagact gaatttttag gtactgtaac acttcagatt acagattctg atatttttat 15540ggttatttat atttatttat ttttgagatg gagttttgct cttgctgcct aggctggagt 15600gcaatggcac gatctcggct cactgcaacc tccgcctccc aggttcaagc gattctcctg 15660cctcagcctc ctgagtagct gggattacag tcacccgcca ctacagccgg ctaatttttg 15720ttatttttaa tagagacaat gtttcaccat gttggccagg gtggtctcgc acttctgacc 15780tctggcgatc cgcccgcctc ggcctcccaa agtgctggga ttacaggcgt gagccaccgc 15840acctggcctg gttacttaaa tttaaataca aaaattatgt tgattaattc tgaatgattt 15900cctgattgct ccccgtttac cattcacaca tttattaaat tcttcgcttg ccatatagaa 15960gcagtctctc tgccatatat gccatataga taacagaact agctgtctgc aaaccactga 16020aattgtgaaa acatctcccc ttttttcctg tttctaattc tagctatgag gattatatac 16080agaagtagtc ctggatttga tttttttttt tttttgatga ttgttttttg atagttgttg 16140actacaaatc atttaaacgt ctgaaagggg aaaggttttc cttaaaaatg gatgacaaag 16200gagaataaaa aggtattttg actatttttt tgaatgatga gttttttttt tctctttctt 16260gttttctttt ggagtcattt atgtgtcact gagtggatac catggaacat gtggcagaag 16320tagatatatg gggtaaaaga accatagttc ataagctcct tgacagaatc actgaagtgt 16380agccgttata tggccactgt cgcaggggga ggcagcagtt ttgaagaagg ggatgagtaa 16440taatgagtga taaaaaggca tcctggatag aagaccaaac tctgcagaag accccagttt 16500gattatgctt ttgttttctg atttgcggag gagagtgaaa atgcctgagg ggtgcggggg 16560agcacatagg gtgtatgtgt gtgtgtgtgc gcgtgcagat tctctctttc actgtatgta 16620tttgtatgca tgtatgtatc ttaggactta agctttctag tcaataaatt gccatagtgg 16680ggaattgctt aattgcttgc cttctgttgt tgtatttaat ttaattttat ttttaatgat 16740ttttttggtg gggtacaggg tcttaactat gttgtccagg ctggtcttga actcctaaac 16800tcaagtgatc ctcccgcctc gggctcccaa aatgctggga ttacaggtgt gagccaccat 16860gcccagctta gttgtatttt aaatgggcct gtttgcagca ttccctactc cccttagttt 16920acctggctca caacctgtct ttccatatca aggcttctgt cacccctggc ccatgtcagt 16980gcatttgggc agcccaccca gcatcatcac ctcatgtccc agggaacttc ctgttcctct 17040cttccagcta tttccttccc tggcagttga gatagtctct acctttgacc tactgttaag 17100ctcagacctt ctgctctcta gttacagcct ctgtgctgcc agattccctc gctcagttgc 17160tttctctagt ttgggttttc tcctttattc agatttccag ctgtttctct cctcccccca 17220ccgcagcctc ctcacttccc tccttatgca tctgagactg tggtcagtca ctttagatgc 17280tgcctctcca ctgtacttgt gtccatcttc ttacctacca cctctagccc tggagcaggc 17340tcttcccctg tctttgtctt cctgggccca ggctcctaag cgctgctgga aaaaaaatcc 17400cccagtattg agcccctaga aatccagtct ttaatcccaa atctgtctcc cccagcatct 17460ggccatcaga tctaaagctt acctgccatc ctttccacct catttctctc acaggggaaa 17520aggagccttt gctcctagag tctgcgctcc tgaccccttc ccatctcacc tgttcaaggc 17580atcttgcaat aaggggttgg tgactctcga ggaatggatc ccaggccctc cctattatca 17640tcttatgtat gccagttcaa cgttctcagc ttcctccagc cgagacggcc cctccagcca 17700ctgctttata ctctccttct ctggttgaaa tttttgaagt aaataggtca ctctgcccat 17760cgttcatctt ccagtcactc tgtgtgttta tcttccaggg aagtgaggct ctatgctacc 17820aagccactga aataattttt ttttttttcc agactgagtc ttgctctgtc acccaggctg 17880gagtgcagtg ccgcagtctt ggctcactgc aacctctgcc tcccggcttc aggcgattct 17940cctgccccag cctcctgagt agctgggatt acaggtgcct gtcatcacgc ctggctaatt 18000ttttgtattt ttggtagaga tggggcttca ccatgttggc caggcttgtt ggcatgttga 18060ccatgttggc caggctagcc tcaagtgatc cacccgtcag cctcccaaag tgctgagatt 18120acaggtgtga gccaccgcac ctggcctgaa ataattcttg acaagatctg cttccttgtt 18180actaatacag tggatatttt gcatcctaat tttaatgcag ttcagtgtgg tagacctgta 18240tttgcatatt gaatattccc ttccctgttt taataactct attttttcct tttcttttat 18300atctcctgct tctctagcta gtcctagacc ttactcatcg gtgtcttctc tgtttgttcc 18360tcaacttgag gagttcctac agggtttacc caatctgctg ctttcattta gcccttttgt 18420tctttttgag ccatctcatt cactcaccca ggatgtagca tcggcccttg aattcagtgt 18480gcacacatac actgtgcact atgggacagc cttcagaggc actttgttcc tgaaattgtg 18540gtggtctttg cctctcatgg agccttgcat atgctgtttc ctctgcctgg aatatcctac 18600cttttactta actgattctc gttcttcttt ccagtcacat tttgtacatt tcttctggga 18660agctttctct gatttcccct ttccacaggt ccaagttaac tgccttgtct aggtcctccc 18720atggccctct gaaggcctcc tttcatagca ccatgtctga gtatactgta ataacacgca 18780ttgctctgta atagcctgtt tacttaccta ttgccaagta atctatcaag tcttataaag 18840ggcggggctg cttttgttct agtcatttgt atctcttagt acccaatata gtgtttggca 18900tatagaaaat acccaacaag gccagtcgca gtggctcata cctgtaatcc gagcactttg 18960gtaggctgag gtgggcggat cacttgaggt caggagtttg agaccagcct ggccaacatg 19020gtgaaaccct gtctctacta aaaatacaaa aattagccag gcgtggtggc gggtgcctgt 19080agtcccagct acttgggagg ctgaggcagg agaatcactt gaactgggga ggtggaggtt 19140gcagtgagct gagatcactc cactgcactc cagcctgggt gacagagtga gactccatct 19200taaaaaaaaa aaagactcca tcttaaaaaa aaaaaaaaag aaaaaagaaa gaaaataccc 19260aataagtagt tcctgaatga atagatgaga atgctgttta gaaggttcat gaattggaaa 19320ccgtgattgc tagggaggct ttgagttgat ggtattgtgt tgaaccatgt gttacccagg 19380atcaatttag attttacact ttgttttctc tgttcctttt tatagtaatt ttctgtatgt 19440ggtgttttcc ccccatgaga ttgtatacca tttctcagcg agaactgtgt gtaatgcttg 19500gtggctccct catggtgcct tgcatggaat tggacttcgt ttcagtggat ctgatcccag 19560ttatgttaat gctcgatgga gctaagtctt atctcgaagc agtccatgtc ttcatcagct 19620ggccctgcct ccatgccctg cacagaccat gccactctgg agaggtagtt tccctgtggc 19680ttattagtct tatgttccag tgtgctggcc aagtatgaga gacatcagtg gtatgagaga 19740gtctctctca ttcaaacttc gtaggttttg tagctgggac tgaccagtgc tgacaggaaa 19800tagaggcatt tattaaaagc cagagatttt tcaagttgca ggaagcaaag ctcttgttag 19860ctatgatttt gtggtgggtt tggtagtcca atataaaagt aaaaactgga tgacaatggg 19920aggagcatgc ttgggtctcc aaagttagat catttttcct aagtaatttg tctttaaact 19980tttactggtt tggaatttcc tgagattttg atcttgccag aaagtttata gcaaaagttc 20040tgagcagatg acacttttgc gtctgaaacc aaatcattgt ttttgttttt aacttttttc 20100ttaatatatt atccttagtt cagccctgaa gattattctg ttatttgtgg atctcaactt 20160tccccccatc tcctggatct ttgtgaaatg aatggtatta attgaataga gaaggaagat 20220ataaacataa acttagtcaa aaacttgttc ttgactaggc aagttgggct ttatagcttt 20280gagctgatga catgtctatt cttgtgaaaa agggattttt agtgttggtt tggcttcttg 20340ttatatttga tttattatta ttatcattat cattattttt gagacagagt cttgctctgt 20400cgcccaggct ggagtgcagt ggctcaatct cggctcagtg caacctccgc ctcccaggtt 20460caagcgattc tcgtgcctca gcctctggag tagctgggat tacaggcggg tgccactaca 20520cctggctaat atttgtattt ttagtagaga caggtttcac catgttggct aggctggtct 20580tgaactcctg acctcaggtg atccacctgc cttggcctcc caaagtgctg ggattacagg 20640ccttagccac tgtgcctggc tgattttttt tttttttttt tttttaggtt tgttttaact 20700ggaactttac gtgaatgtaa ttgaatttag aataaaagca cttaatttca cagtgtgcag 20760tgaactttct gttacttatt ttaacagtaa aaccccttgc agtaaatgac ttggagcaaa 20820gattgctttt ttaaaaaatg ttttaatttg tttttctttt cttgagatgg agtcttgctc 20880tgtcaccagg ctggagtatg gtggcgcgat cttggctcac tgcagcctcc ccgcctccta 20940ggttcaagcg aatctcctgc ctcagcctcc tgagtagctg ggactacagg cacatgccac 21000catgcccagc taatttttgt atttttagta gagacagggt ttcaccatgt tggtcaggat 21060ggtcttgatc tcttgacccc gtgatccacc ctcctcggcc tcccaaagtg ctgggattac 21120aactgctggg attacaagtg ctgggattac aagcgtgagc caccacgcct ggccaatttt 21180tttttttttt ttctttttga gacagagttt cactctgtca cccaggctgg agtgcagtgt 21240cacagtcaaa actcactggc agccttaacc tcctgggctc gaatgatcct cctgcctcag 21300cctcccaagt aactgagact acaggcatgt accactgtgc ccagctaatt gtttttttat 21360tttttatttt ttgtagggac agggtctcgc tattttgccc aggctagtct acaactcttg 21420ggctcaagca gtcctcctgc cttgacctcc caaaatgttg ggattacagg gacaagccac 21480tgcacctggc caaggattgt tttttaagtg aactgagacc cagccttatt agtggtccca 21540gagcagacct gggacctgaa gggaaccctt ttcttctggt ccagcgtctt tcctctgatg 21600ggctactttc ctggagcctt tgattgcctg tcatcagagt aactgagttt gaacagagta 21660ggtagttcct ctccagacca ccacactcac cagctttcat tctgcttctc tcgtttagac 21720tgtggttctg aatcctcagt tctatttact gagtgttttt aaacataaaa atgcctttta 21780atgagattga aggccagagg tgggacagtt gaggacaaag tagaaataaa accttcaagg 21840cggggttgtt ggtgggagtc tttttttgtt tgtttgtttt ttgagactga gtctcgctct 21900gtcacccagg ctggagtgca gtggcacaat ctcagctcac tgcaacctcc gcctcccgag 21960ttcaagctat tctcctgcct cagcctcctt agtagctggg atttcaggct cccgccacca 22020tgcccagcta atttttgtat ttttggtaga aacggggttt caccatgttg gccaggctgg 22080tctcaaactc ctgacctcag gtgatctgtc tgcctcagcc tcccaaagtg ctgggattac 22140aggcgtgagc cactgtgcct ggcagggagt cttatagaag ctgtcgtgga caatgtggga 22200agtagtgagc ctttgtattc cagtatgctg ggctccactg tgcttgctct ggcccccggt 22260cgctctctgt gtgttattga gtccccatcc acggccatac tcttcgtcct gcttctctcc 22320ttaccatcct ctccccgcta gtggtaccac ggctaccact agcaattact gacatgtggg 22380atcttagggc tacttcccta taaggctgca gggcatgtgg tgttggctac gcgcatggta 22440accatggtag ccctgtggtt ctccacatgt gcgccttgtg acctgggatt ggctgcagac 22500tagtaataaa ctgcgtcttc tggtatggaa tctgtctgta gttgtacttt ctacctctgt 22560atttaagggg agatctgtaa cctaccaatg ccagttgaag aggatggatg atagagatgt 22620taacaaacag ctgaaaaact aactacaatg gcctgcaaaa tagaacagca ggtttttgtg 22680gcaaaacttt gtgtccatga gtttgttttt taaatatcct catataatct gttttaaatc 22740gagaggcttt gggtaaaagc catggctagt cttacatgtc atggagtacc tagcttgtga 22800ggttcacagt ttattattta cagagtgtcc ccttaaatct tctttgggtc ggttcagcga 22860atgttgctca gatggacttt tttggctgac atagagtcaa aatggtaatc aagcatgaaa 22920gtacagacag tccttaacgc acaaatgtgt catgcttgaa aagttggaaa gttggttctc 22980tggagctctg attgtattgt cctgtagaat ccgtgttgtg aatggtggtt aaatcccaaa 23040tgagtccgta gaacctatat aatctgcaat atacctgcag tattccaatt aatatgtaat 23100tcccccatag aactatgtta atgatttgta tgtatggtat ttaatattat acataataat 23160gattgtatga ataaaaaaca ttctgggctc catgtggatg atggggtgtg tgtgtgtgtc 23220tgtctatgtg tgggtgggtg tgtgttcata gatccctttt cctgcaatcc tggcactgga 23280attggtttta tcatttccaa ttaagtttca ttcccatgaa ttttggagta cagactgggt 23340ccaggtatgc agggcataga ttagagccct gagaaatagg attaggctgg aattgctggg 23400ttggagatca gtagcttcca ggaacacttt ttgggcctgg ctgtcttcat tatccccttt 23460tgttttctcc tggggtctgc aggtattgcc ctgttttgtt cctctaatat cacttttttt 23520ttttttctgc ttttgaccag ggtttttgcc tctggtctac aactgaatat cctatcagac 23580tctcctgatt ttgaaataaa tatatagttt ttttgaggtg ttctagcgaa tttctaaatc 23640taaatgttgt ggcagagtta ttacatacta attttgctat gagaggttgt agaatcccag 23700atgactaatc ttgtaaacca tacacgcatt tccatctaat tctccattgt atatcatgtt 23760gcagaaaata acagcctcta gagtttacat tgcctccttt gactatattt cttatttaag 23820attagttttc agataagacc ttttcatggc agtacataac tgtacagagg gcttccaact 23880tgtcttggga gctctcatct ctgggagaca tcacattacc cactgccccc tgccccccgc 23940ccccagcctg gatgcactca gcctgtaccc catttctgtc ctcagccaaa cactgctgaa 24000atgcaagagc tttcaattgc tagccagtga agatgcagac taagggattt ccatgtagaa 24060gcccgctctt ttcagctggc tcgtcgagag ctggaggccc cttgcttgtt cacatgaggc 24120tttttgtccc tgacttggtg gctgctgttt cacttctcag cagaaaggga cacccttgcc 24180cccccccaga aaggaagatt tgatgtacca cttccgaaag gttcagtcgg gcatcactgt 24240aaccaagaag ataggtcagg tgaggctgga ggtggaacag ggctgctcgc tagaactcca 24300gattgttcca caagtgcctt ctggcagaga atgatggaag cttccgtgat ttttttttct 24360ccttaatagt tatgagcaca gaagaggagc agattgtctg gctatagaag ctgtcttatt 24420ttttattttt gtttttgaga tggagtcttt ctctcttgcc caggctaaag tgcaatggcg 24480cgatctcggc tcactgcaac ctccgcctcc cgagttcaag cgattctcct gcctcagcct 24540cctgagtagc tgggaattac aggcatgcgc caccatgcca gactgatttt tgtattagag 24600acagggtttc accatgttgg tcagtctggt ttcgaactcc tgacctcaag atctgcccac 24660ctcagcctcc caaagtgttg ggattacagg tgttagccac tgcacccggc cgaagctgtc 24720atattaaata gcactttctg cttttagcaa atttaatcca aatgagactt tagattttct 24780tgctctgact taccagcagt tccttgaaac acatttaatt atttttgcca gaaaatcact 24840caagcactta cgccattttt ttaccgtgaa aatatgctgc attattttaa aatatattag 24900aagtcagtaa ccataagatt ttatatgttt tctaatgtat tctgtaagct ttctgctgct 24960tttgtttgga aggtgtattt tgtaacgtag aggactgctt tatctgcttg taagcttgat 25020ttttgttttt actgtaattt ttttttcttt tgctgtattg agaaatacat tgagtaatta 25080taaagtcagt ggcatgttta taagttaata tttgtatcta ttccttagtt actctaactc 25140aaaacctaaa gtaatcttca actctaattt actctgacat ccagttgact gccaagtcct 25200ccaacttaat ccttatcctt ttttttttaa agagatgcag tcttgctttg tcacccaggc 25260tggagtgcag tggtgcaatc atagcttact gtaacctcaa attcctgggc tcaaatgatc 25320ctcccacgtc agcctctgga gtagctgggg ctacaggctc ttgctaccat gcccagctaa 25380ctttttattt ttatttttta tagagacaga gtctcactgt tgctcaggct ggccttgaac 25440tcctgccttc aggcggaact cctgccttca ggcggtcctc ctgcattggc ctcccaaagt 25500gctggaatta caggcccaat tttattcttg ggatgtatgt ctgaaactct ttccttcact 25560tccttcccaa gccttagttc aggcccttct catctgtggt cttcaaagtc gccttcagct 25620ggttcaggtc cttcctttct gctgtatctt tcatgggagg acatgttatg tatcactgtc 25680ctacttgaaa acttccattc cccattgatg agggtgttac ctccagattc ctaacacagg 25740tgctgaaggc atgcctggat aaaggcactc ccttgatctc ctggccaggt ccccgtacac 25800ctgcagcgca tgctccacat tctgtcttta ctgatgctgt gtcttctgcc tgcggagcca 25860cccaccattc tattcacagc ccctgcctca gcggagcacg tgcctccctc ttcctacact 25920gagctgtcct ttctattgaa tcccctcttt tttgtagtat gggaaatatt ttattatgaa 25980tactcttttc tctgttgcct ccgtgaccac gttaactttg ccctaattcg ccttaggact 26040ccatctgctt aggggaaagt taggatttgg ttacagaaag caagctgcta gaaagaacag 26100tgtttagctt ctgacaggca aaataggatt ttgcaacatg cttttccttt ttaatgctta 26160gacattttat atgaattaat atttttattt ggttgcttat acattacttt ctttttagct 26220agaatgtgaa ccctatagga acatggggat tgcctttcac atctttgtat cctcagtacc 26280taatgttcag tcaccctgtg gtcttgtgtc gtatatacat ttagccttcc ttaattaaac 26340catatgtact ggtccccgtc ccccaccccc aaatagagag aaagaaattc cttgaatact 26400acattgccag tatcaaacca caccttgata tcctctgggg aaagggaggt atcagttgaa 26460aagagaaaag aggttaaaat ctaggcatta aaatgtgtaa ggcttagatg ctggcaattt 26520aaggtatgtt ttcctgaggt taattttgat tgtgtgcaaa ttttacctca tatctaactg 26580taggatttag tcaccacata agatgggata cctccataaa tccttcagaa atgtttgtga 26640aattaaataa agccttattg aagactcagc tcttgagagt catctaccta cctaacagtt 26700attcttgaac agaagagtct tacttttccc tataaggcag tgtgatagcc atctgtatat 26760tcatataatt tatgttggcg cttacttcat ttaaaaatgt attccgtgaa tgcagttgcc 26820aggcggtgtg ctgatcagaa acgtgtacca atggcctctt ttataattat aagaggaaga 26880ccaacctgaa acagtcacac aaatgattaa ttttaattgt ggaggagtgc tgggaaagaa 26940aaataaaaga tgcaatgcaa gtgtttacaa aggagctttg agcttgtttg aagtggtcct 27000tgggcactta agcaaggctt aaagaatgat gtgattagaa gtggcttagc aattctaaag 27060aacacaggga aggcgtgtgg ccagaacatt ggtccctaga gcacatcgcc tcctgacata 27120ccatttcctt aagttaatgt tttaccacta tacataggcc ctcccctttg tttacccaga 27180tttttttaat tttaaggatg tttttaataa cttagaatcc tgtaatttgt tgaacagtcc 27240tgtattccct ttacttatat tccttgagat tttataaaat attttttaca tgtcccaagt 27300cttgattata tctttttacc tcttgttaag aaatacttac ttttctattt ttatgctata 27360tttcatgttt actgtagaaa acaaaaaaag taaaattttt ctttattcct atcactgcag 27420cttataagca ctctaaacat tttgatctat attttgccaa tcatatattt tagttaaaat 27480tgttgttgac ataattgtag attcctgtgc agttgaaaga aataatacag agctgagcgc 27540ggtggctcac gcctgtaatc ccagcacttt gggaggccga ggcaggcaga tcatgaggtc 27600aggagtttga gaccagactg gccaacatgg cgaaaccctg tctctactaa aaatacaaaa 27660attagctggg tgtggtggcg ggcacctgta atcccagcta gttgggaggc tgaggcagga 27720gaatcgtttg aactccggag gcagaggttg cagtgagccg agatggtacc attccactcc 27780agcctgggca acaagagcaa gactgcatct caaaaataat aataataata ataaataaac 27840tttaaaaata aaacagagag atcccatgtg cgctttgcct agttccccca tccactgccc 27900ataacatttt gcagaactgc agtacagtat cacaaccaca atactgacat tgatacagtc 27960tgctcatctt attcatattt ccccagtgtt actcgtatcc acgtgtgtat gcattgtgtt 28020ttcaatactc ttttattata aagctgtttt taatgtgatt caattctagg ttgttttgtt

28080ctgccctcaa aaagcattcc ctctcctaat catatctccg tcataccctt gtatgttttc 28140tttaaacctg ttttaagaaa gcagctacct gtaagagaaa tgagattgaa aacagaattg 28200ccaatctgct tgtactttat aagcctgttg attgtttaga tacggtttag ccagtttata 28260gttaccctgg gtgctgaaag gtatgctgga tgatacctaa ccaacagaga accattgaat 28320gccgttcaaa atggactgaa gcatcagcaa tgtctgaaaa aggcctgaca gtaatgtaca 28380tgtcaaatgg cccgtaattt aagcagagta gagtaagtag aagaataaac atggggaaag 28440ttccagcaac agaggaggct ttgagctttt gctcttcatc ttgagtggat gttgttctca 28500ggtggtaata ggccatcgag ctttctccac tggctgcctc tctggggaac aaataaccga 28560aaagatactc agcaccctgg ttggtacata ggtggtcagt tgatttatac ttcctggttt 28620tcagtgttgc ttgaattttc taaatggaaa cacagtacct ttataatcag aaaacaatcc 28680cgagttttga tttgagggtg ttgtaaaaag ttaaaaaaaa aaaaacagaa atgtgaaaag 28740gaagttgtgt tagagtattt ggagttgaga aagcatgaaa aggacagaag agaagctggt 28800tgtcaggttg catggggtag ctacaagcac actgaccaga aagtcagctg gaaaaaaaat 28860gtagaaacag gagataaaac ggccaagggg ctatacaagc aaacagcaag gacctgagaa 28920gaaaaactag ttaggtgtga ctgtcagagt gatgtgtaca gtgtgatcct ttctgtgtaa 28980aaacaagcag taagaattcg ctgtttacgt ttgcgtgtgt ttggagaaga gtggggaaga 29040gtaggcactg ccagactgtg aacactggtt aggttattgt tatatctttg tattatatac 29100actggacatg ttatttgtat aatatgagaa gaaattttat aaatcattaa atcttttggc 29160atttaggaac atttgtgttt tctaatagtt gcttctatac tattatcttt attatatgcc 29220cttcatcttc tcagtgtttg gctgttgttg tgattccctt ttgtgagcag tgttgaagtt 29280agctaatatt catttcttct cccttctttc accctcctcc agagtctgat ttgaagtatt 29340cctagctgct acctataaaa gcaataagca agattgtttt acttttcaca aactcgtcct 29400gttctgtgcc tctgcctcgg acatagctgt agtatagagt gttgtctccc ttacatcctt 29460ctatcttaga cctactagta aatattaatg ctcactctaa gttcttctca attctttttt 29520tttttttttt tttttttttt gagaaagagt ttcgctcttg ttgcccaggc tggagtgcaa 29580cggcacgatt tcggctcacc gcaacctcca ccttctgggt ttaagcgact ctcctgcctc 29640agcctcctga gtagctggga ttacagtcac gtgccaccac ccctggcaaa ttttgtattt 29700ttagtagaga caaggtttct tccatgttgg ccaggctggt ctcaaactcc cgacctcagg 29760tgatccacct gcctcagcct tccaaagtgc tgggattcca ggcgtgagcc accgcgccca 29820gcctcttctc tcaattcttc ctgaagctct ttctgcacta gattcctcag gaagggcttg 29880tgggaacaat cttctgtgaa tcaacagtac atattcataa tagtttgtca gcagcctatt 29940attttaaggc catttggtct gtatataaaa atgtttggat cacattttct ttctttaagg 30000taaatatgtt attctgttgt cttctggtat aaagcattgc tgtaaatgtt tgacagtcta 30060attatctttt gcttataagt gacttagggt tttttgtcta tgtgcccaaa ggattttttc 30120cctctttctc tctttttttt tttttttttt tttttttaaa cagacaggat ctcaccctgt 30180tgcccaggct ttagtgcagt gaggcagtca gagcttactg aagttttgaa ctcctgggct 30240tgaggaacaa aggatttttt taacctttta attcaaagtc tcatcattta tgcaaccatg 30300tcttggtgtt ggctgttttg ggttgttctc cctcaaaaat ccatgtgctc tttcaatatg 30360tagttttaaa tctttttttt ttaatttcag gaaaatcttg aattagagtt ttccgttttt 30420cgtctggtac attgcttggg tttccttctt caggaactca gcctgttatg tgtatgtttg 30480atcttctttg cctgtcgtct gtttctttca cttcctctca cttttttaaa cttcatttat 30540taaaaaaaaa tttttttttc gagacagagt ttcgctcttg ttgcccaggc tggagtgcaa 30600tggcgtgatc tcggctcact gcaacctccg cctcccaggt tcaagtgatt ctcctgcctc 30660agtctcccaa gtagctggga ttacaggcat gcgccaccac gcccagctaa ttttttgtat 30720ttttagtaga gacagggttt ctccatgttg gtcaggctgg tcttgaactc ctgacctcgt 30780gatctgcccg cctcagcctc ccaaagtgct gggattacag gcgtgagcca ctgtgcccag 30840ccttattaaa aattttaaaa acatacattt aaacttaaca gaaaaattat gagagagaag 30900ggggtggtgc caggcttttt taaacaacca gctcttacat gaactcatag agtgataact 30960cattaccatg aggacggcat caagccgttc atgaaggatc tggccccgtg acccagacac 31020ctcctactag gtccattttt aacattgggg atcacatttc aacgtgagat ttggaggggg 31080caaaactaca aaccatgtca ctcagggatt ggaggagcaa gtaccaccta tactttggac 31140tcaggtagaa aggcaaaata tccaggaaat aagctgctac cgtccagggt tcagcagagg 31200tgcccatcag cctgccaagt actcaagagt ccagcctcta gggagctaat catcatggtg 31260agctcttcga ggcacaggga gctgggaaga cagtgcttgc cacccctgcc tgaatagtgt 31320ttgcacagag agttctgttg tgtcttgatt gggtcctcct gccactggga atgctgtgga 31380ttatactagg tctctatctg gcttgtttca gggctccatg tgaaaacctt cttgatatcc 31440tagccatcca cctgctcagt ccctagtttg caaggaggct gtggggagcc tagattctgt 31500gtcagataga atgtactaca ttccgtctca ggaatgtacc acatcagaaa acagtgcgac 31560ctgcaggaga agtagaggtg aagaggcaca ttcttccgag aaatgtttct ctcaacaccc 31620agcattccct ggatatcagc aggaaattac tcactgctag aaaatgcccc atgagccttc 31680tgttaaggag gtcaagggag agaacagaga aagttctcaa agttgacttg gtcactggta 31740ctttcttatg cggttcttat tttgtttgcc atcgtcatca tcatgctatg tctattttct 31800caatccaaat ccactgcttt caccttggtt ctttctgacc ggtttggcac actcattcag 31860taaatcctta tggagagccc aatgtctgca taattgtgct gtgctgatga ccaagctaga 31920cctacgagtg tcggctcctt tgagatgtac gggacagctc ttctgtcatc tcttctggga 31980agcctctcca ggcttggtga acagtggcaa gatgtttaac agttgtacat gtgtcccatg 32040ttcctttcta agagcctggg caaaccagac ccggtcgcag gtcatcgtag tatggcgtga 32100gcttcctctc tcctttctga ccttttgtgt gatggcaaga acctgcagag tgacacaagc 32160agcaggcttc tgaggttgct ctagcctcag aatggccgtc ccttctccac cctggccctc 32220attgctgagg tttcctttga agcaacagtg ccggaacaga ctaggggaag cagcttggac 32280atagctgtat gatttattac cacccattga ggccaaccaa agtcggcaag gagaggtagc 32340aggtcagtgg tgcctggaag cttcctcttt cctttgcacc agatgtgact gctctgcaat 32400tactcctaaa tttgctactc tcgtttttac tagccaacct tgatgttttt cccttcttcc 32460tgtagaatag acttcccctc tgatcagtac tttctactca acactatttg tggccacagt 32520gggaactcat tgaggacagg gaccatgaca ttactacctg acccatcaac acttggcata 32580acttgaaatg caaggacaaa aattggctgc aagtacaatg tggtcttcac tctgaaggtg 32640atccttaaaa cttggctttg gcatcatatt gccttaatat acctagggga ttgggtaaaa 32700ccagttactt taaaagagtt ttacaattct ggccttctag ctatcttgtc ttcttaaaca 32760agagcacaag atgaatgtat cttagtgaaa ttttatatgg tttgctttga gtaatcttgc 32820gaagattgat ttttagcaca gtaggaaaga cacattctaa tagtgatttt tttccccgag 32880tttatgtact gctgttgcat gaaaatctga ctagatttaa tgttcctaaa gttctttgtt 32940catcctgatt tttgcaggtc ctagggaaag ctttgttttc ctcttaacct aacttagatg 33000ttgtcatttc atgagctttg gaggaagagt gtatagccaa ttgtgtaatg tctttaaagg 33060atattatctc tgcaatagtt gtttataagg cctaagttat tcatgtaata atagtggccc 33120cggatctgtt tctagcaata ggtatatgga ttttggttcc tatatagttg tagttgtggc 33180tttgagatat tgagcaagcc cttttaagaa aggatttggc atccctcagc cttcaaaagc 33240ttctcaaaat tgatcatatg ttattagcaa aggtttactg cctgcttcca ttgtatagac 33300aatttatttt ttatgtattc cgttctaaga aggcagatga ccaaaagatc ttgcatctgt 33360tgcccaaggc ttgtgactag agaggaaaga gataagaata cttttttaaa atcccatttt 33420actaaatatg ttgaggaagt ggtaagatat attaatttgt tgagattttt ctgttatgcc 33480tattatatga aataggtact ctgaacatgg cttcttaatt aaatatattt gataaaatac 33540aacttgcttc ccctggagtt tagaagtcag ataactgcca tggagagcta tgctttcttt 33600gttttaaaga tctgcttatg aacatgataa acaggaacaa tttaatgttt tcaatatttt 33660cttgtatttt actgcaagtt tatacacaac ataaatatgg gggaaggggg aaatgtttat 33720accagagcca tcctgcccat tctttcctta cagaaggaca aaggagcagt atttatttta 33780actacaaaaa tactattgta ggttttaaaa attccgtata ttttgatatc ttgtgttcct 33840cttgaccttt aatttgctaa atagttgcaa agaatgaagg taacctgcat catcttctta 33900aaaaccaact ctatctaatt ataatagttt gtctatctct gaaaaatagt gatgtgttca 33960ttctgaaatc agaactaccg gatgcagctg cattttgtta ctatttgaat ttcgggagag 34020ggaggaggat gcagcctttc gagctgctga aatacacaaa cacaaagaag acaccaagca 34080tagtagaact gtgttaagct gaccaagcca gaagaagcac ctattctcag catagtatga 34140gacgtaaagg caatataatg ggcatagttg aagatggtag aaggaaaata gactctgatg 34200gtttaatgtt aaatgctttt tttaaaaaag tggtattcca atatcgaaga agaagacttt 34260ctacttttag aagcaataaa ggaaattgca gaggaaaggg tcaataggtt ggaatacata 34320aaaattaaaa acttttaaac tttttttttt tgagacagag tctcactctg tcacccaggc 34380tggagtgcaa tggtgcaatc tcggctcgct acaacctccg cttcctgagt tcaagcaatt 34440ctcctgcctc agcctcccga gtagctggga ttacaggcat gggccaccac tcctggctaa 34500tatttgtatt tttagtagag acagggtttc accatgttgt ccaggctgat ctcaaactcc 34560tgacctcgtg atccgcctgc ctcggcctcc caaagtgctg ggattacagg catgagccac 34620cgcgcctgga ctaaattgtt tcagtattaa ttttttttaa aacaagatct tactgttgcc 34680caggctgaag tacagtggcc caatcatggc taactgcagc cttgacttct gggcctcaag 34740ggatcctccc acctcagcgt cccgagtagc tgggaccaca gacatgtacc accacaccca 34800gctacttgtt ttatttttat ttttgtagag atgaggtttc accatgttgc ccaggctggt 34860ctcgaactcc tgggcccaag caatcctcct cccttggcct cccaaagtgc tggtattaca 34920ggtgtaagcc attgcgccct gcctgatttt ttaaatgtgc aaacagataa gttggaaaag 34980tgatttccaa taaagataaa gagttgatgg ttttaaaata cgtaaagagc ttatatgaat 35040gagaaaaaca ctaacattcc aaaagattag aaggcaaagg acagaaagaa acaaatcact 35100atgtctggga agggacatga aggagcaggt tcccactggg ccagcggggc tcaaacccac 35160tggggacgtc cgagagactg caagggccat gccttcacat tgccgtacct gagaagcaag 35220gagctggggt atttatctct ttcacacttt gggaggctga ggtgggcgga tcacctgagg 35280tcaggagttc gagactagcc tggccaacac agtgaaaccc cgtctctact aaaactagaa 35340ataattagct gggtgtggtg gcacacacct gtaatcccag ctacttggaa ggctgaggca 35400tgagaattgc ttgagcccag gaggtagagg ctgcagtgag cataaattgc accactgcac 35460tccagcctgg gtgaaactct gtctcaaaaa gtaataataa tcatgataaa taaaataaca 35520ttagattgtt agcagaagta gccacaggtt tctcccacct ctctgcaagt tgctgagtgt 35580gattcccatc aagaggtaca atgtcttttt atttttattt tatttatttt atttatattg 35640cctatgttgt ctaggctggt tccaaactcc tgagctcaag tgatccttct acgtcagccc 35700cccaaagtgt tgggattaca ggcatcagcc actgcacctg gcccagatac tttttcttga 35760gtaggaattt cgagtcaccc tgaacattgc atgccttcgt agtggggaag acaataggaa 35820accacaggct gtaggctaaa atgggttgtg tttcttgtaa cgtcatgaca aggcataacc 35880catcttggca tagtaaatag taagcactca ctgaactgat gattttaaat ctttgctgtt 35940tattcagcaa tatcctaaat tagcgctatg ttagtggagt tgcatctccc tcatggatta 36000gtctgaaaaa gatgagaaat ctgtatgtag accaagttat ccttaaactg ctcataatgt 36060atgatgcacg tggttttacg tgtacagcct ggtaccattg ttcttaggca catttcagtg 36120ccagaactct taatacccag gaagaagcaa aaagaaagat ggaggtgcag ctagaggttg 36180tggcctttga acgattcatt ctgccttaat aagagtggtc tggctgagct cggtggctca 36240cacctgtaat cccagcactt tgggaggcca aggcaggcag atcgcttgag cccaggagtt 36300caagaccagc ccaggcagca tagcgagacc ccccctcccc ccgtctctac aaaaaaatag 36360aaacaatgag ccaggcatgg tggaacgtag tgcgtggtgc ctgtagtctc agctacccag 36420ttggctgagg tgggaggatc acctgagccc tagaagtcga ggcttcagtg agcccttatt 36480gtgccactgc actccactct aggtgacaga gcgagacagg tcctgtctcg aaaagaaaga 36540agaagaatta aaaaaagtga ttagatccct tgtgtttggg acacttgttg gcagcaggga 36600tggtagcgtt tatgagggtt gcatgtaaca tcgcctagct cagacatctg tttgactgtc 36660ttcccccctg aagcgcaggc tctgtgaggg caggtctttt gtctttcttg ttaatcttca 36720tatgcttagt gcttgccaca tagttgatgc tcagtcgata tttggatgaa ttgaagggat 36780taatgcattg aatctgaacc ttgctttctt aatgcatatg gggagttctt tggaaagcca 36840cacagaggag cttggttgcc tgcttcctct cttccccaga ttgtcttttt attgttgtgg 36900cttcactgaa gcactctcac ttcaaataat tttgggcatt ggtcgtattt tattctttgt 36960tccttcttca tccttacccc tcagatggta tgtagaaaag tacactacat ctagaaagta 37020ctttataaac tcatttggtt gataataata catatgcctt ttccttggtc ctggtagcag 37080aatcttgtgc cactcttgga atacaaacga aattcttaac caaagccagt ttcattttga 37140tgttctattt tcctcccatt cacactccaa attgtgcacc aaagtatcat cctagttttg 37200tgaggatggt tctccatact tcagggtagg agtatcatgt ggattcctat gatacctttc 37260tccctgggac catggagggc agcagctggt gattgatagt ctgattcccg gtgaggaaag 37320ctgtgagcct tccacttgca gatgtctgcc aactacatgt gtccttagtc aactgtacca 37380ctgtcctccg gcaaacagca gaagcccagg gcctgaagtt cttaagctgt cattatggaa 37440agcagaaggt aaacaaaaca gaagtgaaag tagatttaat tttttagact gttctcttac 37500aggaatggtt ttgtggttct cagcatttta aaaaaaatag tggttccaat atgttttatt 37560gacatcaatt actgtaagtc tgattcattt tctgcctatt gatttctacc caaggtgaaa 37620ttcatgacat ttaacagaaa gcataagtga ttttttaaaa gcagacacta ttagggacgg 37680taaaaataag atttaaagtc gggacacttg aaaaagcaat ttttatacct ttggtaacga 37740ttctattctg attctttgta taaataatat aaacaaaggc tctagaagct tactataatg 37800aagttggtgt gctgtttcta aattctggtt taaggcccaa attcatttta tctgcattaa 37860cttttttttt tttgagagtc tcgctctgtc acccaggcta gagtgcaatg gtatgatctc 37920ggctcactgc aacctctgcc tcccgggttc aagcgattct cctgcctcag cctcccgagt 37980agctgggatt ataggtgtgc gccaccacgc ccggctaatt tttgtatttt tagtagagac 38040ggggtttcac tatgctggtc aggctggtct caaactcctg accttgtgat ccgcctgcct 38100cggcctccca aagtgctggg attacaggcg tgagccactg cacccggccg tgttaaaatt 38160tttcagtggt agaccactat gtcaatatgt tgctttcact gacaacagta ttttcttaaa 38220gataggatac cccatttcta gatgaatctc attctagctg gaaaataatt tttcagttct 38280gaaactacat caggcctcag ggaatcaaaa ctagctatta gccacacaca tataaagtgg 38340ctttgcttta taaacgattt agggtcacca tcaatgacaa tggtcccttt ttattgtatt 38400tttaagagtt tcttatctta aatggctgca taactgtaga gttttaaaaa aattaagtaa 38460atgaccatgt taatgctcta ttaagcttcc aaacaatatt gtaatttact ttgaagattt 38520ttttttattc tcaacatcct gcagcttgac cgtttgcctc cgtgtctcag tgctgcttat 38580tttgaggtgt ggactggagt ccatctgtcc cccttgcctc tgaactgctc cgttttgtgt 38640ttcgtaattc ttcatgctgc atcctgggcg catttctctg tagtagcttt caatttgctc 38700atgctttgac tgggcttagt ctagcgttta tcctatctct taaggttttt taaaaaattt 38760tcatgattat tcatttattt ccaggatttc tcatttcttc agtcacatct ccttgttctg 38820gttttacttc ttcctgtttt tattcataac atctttttta tacacgattc cttcatgtat 38880ttctaatctt aagtatattt aattgcttat ttgattcttt ttttttttta ttgagacagg 38940gtcttactct gccaccaggc cggagtgcag tgacatagtc atagctcact gcagcctcaa 39000ctacttggac tcaagcgacc ttcccacctc agcctcccag gtagctagga atacaggtgt 39060gagagccgcc acacccagct gatttgtctt actatgttgc ccaggctggt cttgaattcc 39120tgggctcatg tgatctgccc ttcttggcct cctgaagtgc tgagattata ggtgtgaacc 39180actgcacctg gccaagtatg tttatttatt tattctaatt tgagagggag tctcgctctg 39240tcgtgcccag gctgtagtgc agtggcacaa tcccagctca ctgcaacctc tgcctcctgg 39300gttcatgcga ttctcttgcc tcagcctcct gagtacctgg ggttacagtt gcgtgccacc 39360acacctagct aatttttgtg tttttagtac aggcggggtt ttaccctgtt ggccaggctg 39420gtcttgaact tgtgacctga agtgatccgc ccgccttggc ctcccaaagt gctgggatta 39480caggcatgag ccaccacgct tggcccaagt atgtttattt ttaaagtccc caacaagcta 39540tacaataaat tgcatatgga atggattttt gttctagttg atttgttggt tatcatttgt 39600agaactaact agttgtcttc tgtgtttgat accttgcttc taggtcattt tgagttggga 39660gccttttgtt ttgtttttat tctcatgctg tttttgagcc tagctgtgcc tttatggttt 39720tctctaaatt taattgacca ttgttttata tttggagcag tgggtgtaca tcagagtgtg 39780aaagcagccc caccctctcc accagaaggt ctccatgcca gtttcacgaa gcatttttca 39840tgccctcatt cctgccctta tcccttgatt tgtggggagt ttgtaaagca gttgattgtt 39900ttttttccac gtagttttcc aagtgcacat aattgttctg ttagtgactt gtagctccat 39960tatctattaa ccttgcccca gaccactgta caagcggacc caacgcttcc tccagctgtg 40020gcagggacag ttacttggta tcctgctgcc ttttcaatgc tgaccagttt tgccccttcc 40080tcccctcaac ccctgtcttt cattcaacta tcaccaaacc aaaagattct ggtttgcttt 40140ttagtatgtg ttcttattca gtacatagtc attttaaaat ttaaaccaaa acagacttgg 40200tactgattag cttaatttta agctttttct ttattattaa acagtgtagt ttatcttagc 40260atttcatatt aagtatatga tttatttcat attgcttata tgaatgtaca cataaatata 40320ataaaaatat tttcctaagg tttttgtagt aaattatatc gtttcattaa ctttcatata 40380tagcattgct tttgacctgg aagacattga acctctgatg atttgtatat tcctcggagt 40440atactttgtt acatagaaat tttctcattt ataatgagat ttgtgattaa caaaatttgt 40500tcaacatgca ttactttgaa gatctggttt ctaaaatttt atgctagtta ccccaccccc 40560ccttctatat atatctccct attcagcgac tactgcaaga gttccaggaa atgtacactg 40620tgtgttcact tactgcattt taaatcattg cctttactat atttctgcat ttcccttcaa 40680tctagctctg tctgtacatt tctgaaagcc agtagcttcc ctgaagaacc aggtaacaac 40740ccgaacaatc aaattagata accatttgta gaatggaggt tccgggagat cttagaagat 40800gtgatgggtg ctaagggact ttgtagttcc ctgaagttcc agtgagtaaa aggtaccctt 40860ggaatttttt attccttcag acttttaaaa cagagatcac tttcaaaaat tactctttct 40920gctttgaatc catgttttag taactatttt gacactgttt ggtcagaagg ctgtgtgggt 40980caactgcaaa taaataaaat aaatgtgatt tcagtaattt ccattttgta acaagtaatt 41040gagaaaatag gattggatca gatatttgct tatacacatt ccctttcagg agcacttctg 41100ttctataaag aatgttggta tattgttaag gacacttcaa gctttgggaa cctttgaagt 41160atccattgat tcagttaaca aaattatgtt gagtgcctac cctgggcctg ggcctgtgtt 41220aggaggggac actaagatga gagtccaaag cacttcttct cagactcctg gctgctaatg 41280ggttgctgcc tctacttctt cacttagcag atagctttaa aatgagtaat gcattttacc 41340atggagcccg taagagacat tcacccagtt gtggaccgag gagaagggtg ttaaacccag 41400attgtgatgt ttcacttgat gaagtgctta atataaacat ggaaatattt ccgcaaggat 41460aaactggctt ttatgcctgt gtgttttcag gagaaataga aatctctaat caaatattgc 41520cagcttttca cccaagtttg actttttgcc taattgagtt tgggaggtgt ctgaataatg 41580gataatgagc tttcctgaat aaatataaaa attaattaac tccaggctct aattcattct 41640gttaccagag ttttgtaagc atgttacccc tttgtgttca ttgggagatc atctgttacc 41700ttcttaaatg agtggggaag gatgggaaat gaggaagagc tataaaaact attcaggtga 41760agaaggtttc tgcccctcct tgcccctttt aaaatctcca gctcagcaga tgctttgttt 41820aaacttgatc aagtgcttgt gaatcttcct agcctagcta aatcataact ttggaaggac 41880ttgctttttt ctctcatgac aatggtttac cacagaaatg attcagatca ctttgtgtgc 41940ctgatgccta tgtaaaatga tacagtgaaa tggaaaccat ttacctgtaa gctttgggca 42000cacccaagcc tgcttcagga gcacatgatc aggcgtgcac tctgggagag ccgtacacat 42060ttgacatcta tgatgtgtgg cgttttattc tatcacattt ctgaaatcta cactaagaga 42120aaggaggctc ttaaaaaacc actgaggtgt ggactggggg aaggagagat ccgtaaagaa 42180cctgtttgtt acctgttgat actatttccc attggtaaaa tttctaattt agtgtgatcc 42240agccctgaaa tgctgaggca cacactgaat gactcctgac atctttagtg tttttgttca 42300ggggactctt ctgggaatct gtttcatggc aagtttatta ttcccttttg gtttggctca 42360tcagtttacc cagcagtcat cttaatcggt tttaaaggct tttattttat tttgttttct 42420ctgtggaaat tttacacatt cagtagatta gaagtagtta tttaatcttt ggttagcata 42480ataaaagatc ttctagggac attttttgct tgcagtggaa ggctagttaa atgtgttcat 42540tagtcatgaa tctgcttttt ctatagctgt tggaaacgta gctcccctgt gatacagttg 42600tagaatacag aaatctcgtt ttgctgttac ggtacggtag tctacttact ttcttccaaa 42660ccattaatgt tatagttacc tttaattgcg taggtcctat cacccctcaa ttttaagact 42720ctaagcctgg cattttatct tacaaaatga aatataaaga cttgtactca gagtatgtgt 42780gtgttttcca tataccattc taaagtagag aaagatgagg gattcgccag aaactgattt 42840ctaataaatt atccagaaac tgaccccttc tcacctcttc tgttactgtc actgtggttt 42900cagccacagc atcctttgct gcattgttac cttagtttcc tgactgtatc cttccttaca 42960ccattgatcc ctgcaatccc atctgcgcgt agcagccaga agggatccac ttactgctgt 43020gatcagaaat cctcagccag gtgcagtggc tcatgcctgt aatctcagca ctatgggagg 43080ctgagactgg agaattattt gagcccagga gtttgagacc agcctcaaac tgggtaatat

43140aatgagacct catctctaca aacaggaaaa aaaaaatttt tttttttttt ttaactagcc 43200aggtatagtg ctaatatacc tgttctggga tccagcatgc tctccctgac ctgcagcttc 43260atctccacca ctttgcccct cactcccacc acaatggctt tcttctcttc ctcagacatg 43320ccgtgcgtcc tcctacctgg aatattcccc tccaaacatt cccatggctc actccctcac 43380cttcatcaga tctctgttcc agtgtcactt ttactggaag gtcttttgtg accatcctac 43440ttattataaa aaaataatct gcccaacctt ctccttttat ttcctctact tgatttttca 43500atttagtact tatcagctga catatatttt gtctctctgt ctctctctgt ctctcataga 43560aggtaaattc tataaaggaa ggaattttta tgtttggttc tttgctgtag ctccaatatt 43620caaaacagtg cctgacacac agtaggccct ttatatttgt tgaataaatg ttgacactct 43680gatatctaat ttttgtctgg tgactaatac gaaaactata gagtgataat aaaagcatta 43740ccttagtaga ctggaaaggg atgagcgcta ggatgaactt tctgcctggc gatcttgctg 43800aatttaggag gcagattggg gttcaaagga ggctgaaatg gctaggattt gcagagcagg 43860gtactaagga tgagcaggct atgacagaaa gaactccaga aatctgcaaa gggatcacct 43920tgagtctggc tggatacagt gtacactttg tagggtgtct cttcatgagc ttggataaag 43980aacaactgtt ggggagtgga taattcccag cactcattca agcttgcatc ggccagaacg 44040gagagagaca gacctctgta atacgtagga tatttggtag aaacattcaa ccgaaaacca 44100tcagatatgc aaaaagtaat aataataagt aaacaatgtg atgcatagct agaagaaaaa 44160tcagacatta gaagcaagcc cagaaatgac agatgataaa ttagcagata aggacattaa 44220aacagctatt ataaataact tagcagattt aaagaaaaac aacataatga ggataatgga 44280agaaaaacaa ccgaatacca tttctaaaga agaaaaatac aatatctgaa atgagaattt 44340agctggatag gattaatagt ttaggcactg cagaagaaaa aaacagcatc tatatgagaa 44400tatacccaag ggaagtacag agaggaaaaa aatgtggatt ggggggtgcc tcagtgacat 44460atggaacaat attaaacaag tctgccccca aaatacttga aggaataagg ttcaagtttt 44520ttccaggttt aatgaaaact ataagcctac agattcaagc atttcaacaa accttcagca 44580aaataaacaa aaccacagta ggcctggcac actgtctcat gcctgcaatc ccagcacttt 44640gggagcctga gtcaggagga ttgcttgaga tctgcttggg caacatagcc agaccctgtc 44700tctacaaaaa ataaaatgaa ataaattagc tggatgtgga ggtccacacc tgtaactcta 44760gctagcctgg aggctaagaa gggaggattg cctgagccca gtagttcaag gctggagtga 44820gctaggactg catcactgca ctccagccta ggcaacagca agaccacatc tctctctctc 44880tctctctctc tctctcaaaa ggcagtgaaa taacgactta tttggggaaa aaataaaggc 44940agagaatttg ttgccagcag actagcataa aaaaaaggaa gtccttgaaa cagaagagaa 45000atgataaaag atggaaattt ggatatatac taaagaatga ggattgctaa aagtgacata 45060catagataaa tatgaaatat atttttattt taaaatttat ttaaagcaaa aataaaaata 45120catcatattt ataacataga aataaaaaat gtatgataat agcataaagg ataagtggac 45180aaatgctgtt gtcgtatttt tggtaaaatg cactattatt tgaaagtaga ccatcgtgaa 45240ttcgatgcat attgtaaacc aaatagaaca ctaaaaaatg aaaataaaga gatatggcta 45300atgtgccaat ggtggagata agatagatgc aaaaaaagaa aaacattcaa aagaaggcag 45360agacagagga aaaaaggacc aaagatcaaa tgagtcaaat agaaagcagc taaactagca 45420atatggcaga tttaaatcta gccatgtcaa tagttatatt aaatgtaaat gttctaaata 45480cctgaattaa aggatgaaga ttgtcagatt agattgaaaa agcatgaccc aactacatgc 45540tgtctgtaag aaattagaaa aagaacaaat taaatccaaa gtaagaagaa aggaaataga 45600gtagaagtta gtgaagtata aaacaaagag caaagaaaat caattaaatg aaaagctggt 45660tctttgtaaa gatcagtaaa attgataaat ttctagctaa actggccaag aaaaaagaaa 45720agacatacaa attaacagta tcaggaagaa aaacagagaa ttcaaaggag tgtaatgcaa 45780actttatgct agtaaatgca ataagttaga tggtatggaa aaaaatgtga acaatacaaa 45840gcagactgtg gttgcctttg gtggcagtag cggggtggga gtggaaggtt gaattgactg 45900gaaccagaag cacaagtgaa ctttttgggg tgatggaaat gttttgtatc ttggttgcat 45960tgatagttaa atggttgtag acattgctta aaactcactg aacacttaag tgggtatgtt 46020ttattatttg taaaatatac ctcaaaagca gttttaaaaa tgtattcaag tacatactta 46080agatctttgc attttactct gagtatacct taattttaaa atctgttttt taaaaagtat 46140tatgtagata ccttttattt tcccaatgtc tttattaaat gacatctcca cgttttgctt 46200cttacctcta tttttttttt tttatttctc tgtctctcag gcatgcacac acacacacca 46260aaaaaagtac atatgcataa tccttttggc tgaataaaat cagttgcaac tgttatttcg 46320gcccttattt gctccgggta aatattcgtt agctgagtgg tttatctgta tcagatattt 46380cttacatctt catccagtca caccagctgg actgaccaga ttgtttttca cttcaagggc 46440agaatttgta ctcactgctg aatgcttcca aatgatacgt agaataacaa atttaagact 46500tagattttta ctttttcagg tctttttttt tttttctgtg ctgtatagca tttccctgaa 46560agcttaatct catctgtaag tgatgcagtg gatgtgttac tattggatta atttatttac 46620tcttaggtag gtttgtaatc tgtcatcatg ctgttgtttt tttgtgtggg tttgtttttg 46680gttttgagac agggtctcac tctgctgccc aggctggaga ggctagagtg cagtgatgtg 46740tttatgggtc actgcagatt caatctcctg ggctcaagtg atcttcctgc ctcaacccct 46800tgtgtagatg gaagcacagg tgcacgccac cacacccggc tattttttta aatgtattgt 46860agagacgagg catcattttt ttgcccaagg ctgatcttga actcctgggc tcaaacaatc 46920ctcccacctc ggctcccaaa gtgctgggat tacagatgtg aaccaccact cgagctccat 46980cattctgtta ttagttgttc tctagtatga gtcaaaaact cttacctgcc cttttacagt 47040tttataaata agtaagcaga atagcagaat gtggacattt tttaaatcca aattgaatat 47100gcacatgact caaggagtca aatagtaccg taatcggttt atgataaaat ccagtggttt 47160ggctgggtgt cgtggctcac acttgtaatc ccagcacctt gggaggctga ggcaggtgga 47220tcacctgaag tcaggagttt gagaccagtc tgacctacat ggtgaaacta ctaaaataca 47280aaattagctg ggcatggtgg tgcatgcctg taatcccagc tacttgggag gctgaggcag 47340gagaattgct tcaacccggg aggcagaggt tgtggtgagc cgatatcgca ttatttcaga 47400acaattttcc acaagatcag tgagtgctgt ccaatagaca tataatacaa cccacataca 47460tgactttaca ttttcttgta gccatagtag aaaaggtcaa aagaagcaga tgaaattaat 47520agcctgggca acaagagcaa aaccccatct tttaaaaaat aaaataaaat atggtggttt 47580gctgtcccca cctcagacca tttctctggt ctttctcatt gaccaccact cccaatcttt 47640gttctgctga ttgattacag cttgtatata tctccatatt tctaagcaaa atgtttatct 47700tttttaaatt tataaattct ttttattatt tttcagagac agggtcttaa ctctgtcgcc 47760caggctggag tacagtggca ccatcgtagc tcactgtagc ctcgaactcc tgggctcaag 47820cagtcttcct gcctccgcct ctcaggtagc tgagactacg ctacaggcac ataccaccat 47880gcccagctca aaatgtttat cttttgatac attattcgag accattatta aggtggatga 47940tttagttttc ttaaacagcc atcccctttc ttttcctccc ctctgcttca ccgcccccat 48000tttcccaatg ttttaccttt tggttaaatc agtactcatt gtttacatta tttgcctctg 48060cacatagtca cagatagtat tgtactgtac tgtactgtgt ttctttttta aacattattt 48120ctgttgttaa taattgactt tttaattttt ttcctatttt gttttttaaa gagatggggt 48180cttactatat tgcccaggct agagttcagt ggctcttcgc gggcatgatc ccactgctga 48240tcagtacagg aatttccacc tgctccattt ccaacctgga ccagttcacc ccttcttagg 48300caacctggtg gtcccccatt cccgggaggt cagcatattg atgccaaact tagtgcggac 48360acccgatcgg cataacgcat gcagcccagg actcctgggc tcaagcagtc ctcccgggct 48420caagcagtcc tcccacctaa gcctcccgcg tagctgagac tacagacact tgccaccaca 48480ccaggttaat ttttgtgttt tttgtagagg tggggttttg ccatgttgtc cagactcatc 48540tcaaacttct cagctcaagt gagcctcctg cctcagcttc ccaagtagct gggattatag 48600acgcatgcca ccacacccca tgataattgc cttttttttt aatttgcata attttctttg 48660tagcttttgc taatgttccc atatcttctt atagccttac agaatgattt tccacaagat 48720cagtgagtgc tgtccagtag acatataata caacccacat acatgatttt accttttttt 48780gtagccatag taaaaaaggt caaaagaagc agatgaaatt aatagtatct tttacttaac 48840ccagttcatt caaaatgtta tttcaataaa tggtcaatat ttaaaatact tgagatattt 48900tgcttttatt tatttctttt gttactaagt cttcaaaatc caatgtgtat tttacactta 48960cagaacatct ctttttagac tggccacatg tagctcaggg ttactgtatt ggacagagtg 49020gtttcagttt caagtttttc cttggagaca tcctacttga aatttccatt ctccatgtat 49080ctgggtggtt ggtctataga cttgccactc acagctgtca tcttgagact ttctttgctt 49140ttcttctcta ttggatattc agtttcctgg atttcaggtc ttctcatttt cctctagtag 49200ttttgttagg tcatggttgg tatggcatgg ttgggatagc gtgttcacac agctatctcg 49260tgagtcatac tcctccaatc cagcctgctc gcttcccgtg tctgtcatgt agttgtcacc 49320ctgctatctc tccctccagt ttttgcagaa atttcctttg tcttcactct tggtcttcct 49380ctcccatccc ccatgtatcc tatatctttc tctttcttgg tttatttcat cactcaggtg 49440gaaaagatgc tccagtggat tactgggaaa agggggagca tggatgataa aggtattgag 49500accttacacg tcagggaatt tttttttttt tttttttttg agacggagtt ttgctcttgt 49560ccaggttgga gtgcagtggc gccaactcgg ctcactgcaa cctccacctc ctgggttcaa 49620gtgattctcc tgcctcagcc tcctgagtag ctgggattac aggtgcccgc caccacgccc 49680agctaatttt ttgtattttt aatagagacg aggtttcact gtgttggcca ggctggtctt 49740gaactcctac ttcaggcaat ccacccacct cggaatgttt ttattgtccc ttctcatttc 49800atgactgctg ggctaggtat agaattccag aatcattgtt cttagaatct cgaaggcatt 49860gcttcattgc tggccagctt tcagtgttct tgcaaagtct gaagctgtgc taatcacctc 49920atcctttgaa agtgaactgt tttttcttcc cagaaactta cagaacattc tctttgtccg 49980cagaattctg ggattgcaat tactgtgcct tagaatgggt ctgtttttat cattatgaag 50040agtactggat gggtcgggag gttttcttga attacttctt gatgttttct ttccttgtat 50100ttttttgttt gctaattttc tatttttttt tcttggttta ctttcttggg cagggggatt 50160tcttctactt atatttgatt cttcagttga gcttgtcatt tttgctatct tgtttttaag 50220tttcgagaga catctttgtt ttatataaca ttctgttctt aatacataga tgcaagatct 50280tttctttctg agtatattaa tatgtatttg aaatctttct attctctgca gtttgtttcc 50340cccaagggtt tttttttttt tctggttttt gttttttgtt tttatgttag agactttcct 50400gttatatctg gtcatcagtg gtacctgcat gtggtggaga gtaggggctt attggagtat 50460gagaaccttg agcaggtgta aggagcctgt caacactgcg ctggcctcag ggcctctagg 50520gaggctgcca gttgtgcatt ctgaggatac cttttggttg tgccttttgt ctggtcagat 50580tatctagaga tgctctgcct cctacctgga ggagaagggt ctagctgcca gcggtgtgag 50640tgtctcttgg ggaaaaggac tcgagttcct ggtgtttggc ttgtgtatgg ccgcttaccc 50700catttttggt ggagcgctca catcttccac tgtgccaaca gtcttgctgc agttcataga 50760ccttctggtt tacatttttc cagaaagtat gtctttagat ttctgcagaa gtctgaggag 50820catggaagga gcttggggaa tgagatggca atccaggtct tcccagatgg ctctaccttt 50880atcccctgca gggaatccca ctcctccttc ctgactggga gcacagccag agccttggga 50940ggaatctgga gtggaaatct cgggcggtct ggctttctta ctgttcactt gtaattttgc 51000tttctcacaa ctgccaacca ctaatcagcc tgatttccag cttccagaat tctattgctg 51060ttgtctgctc tcctattccc accgtagggg atggggctgt cttttttttt ttttttaatt 51120ttggtaaaac atacaaaaca taaagtgttc cattttagcc atttttaggt acacagttca 51180gtggcagtaa gtacattcac gttgtgtgta tttgtttttt tagtaataaa caatataaaa 51240ttttttaagt aataaaacac aaataaaaga ttgtttaatg tgattatcgt ggaattttag 51300gtgtgatcag gagccatggt gtagtcttct gttgaaacag ggtgatagga tttgtttacc 51360acctcctagg aaagcagttg gatagtttgt tggcataaaa gtacatttta tctattttta 51420ataatcgtag ctttatagaa attgcagttg gaactcccag gcctggcatt caaggctctc 51480tgagatctgg gctacccacc catgtcctcc agccgtctgt cgcacctcct actgcccact 51540cactgttcct ggcatgagat gtgatctcca gcccccatgc ctttgctgtg cagggtgttc 51600cagagtgaat tgtccctcct gtctgtctct ctgccctctt cctcgtcttt ccatcttcct 51660gccccacatc actgcctcct acccaaggcc tgtgctcatt cctcctcggt tttcccccat 51720ggcctggtac atacctctga attatcacct tgcatttccc atattgcccg gctctctttg 51780atgtctgttt ctttgctggg tcttcctcag tgtctgacgg tcagttaaat gtctttattc 51840ttttttgtag gatatccgac atgaagccag tgacttccca tgtagagtgg ccaagcttcc 51900taagaacaaa aaccgaaata ggtacagaga cgtcagtccc tgtaagtatc cacgtggccg 51960gtaccagtct tgctcttcct ttgctgcagg cctttttagt caagactcct ttcgcctcag 52020ggtttagtat aataataaat caatgtagca gaggtttatg acgcgattgt ttcctatagt 52080aaaggcatta gagacttata gtaatagctc atttttccac cattatagaa gggctcaggt 52140ttcagtttct ggaaaattca gtgaagttca aagcactttt cttaagcttt gactgttttt 52200gtgatgaatc attttcctac cagctgaagc agagtatagc aggcataata aaaccttttc 52260tggatgactc agcagcagcg tcattagggc atgagcactg tgttccgctg taatgaagcc 52320ccgcacaggc attcggggtg ggcactgtcg tcccctgcgc tgaatatgca aggcagctct 52380gtctggagtc cccaccgcct ccacccccgc caacctcatc atttttctcc ctctttcctg 52440ctgttagttc ttcctaggat tgtcagtgtg cctgctggcc tgtggcagcc ctgtccgcct 52500tctgagtgat tggctgtcag tctgccggta gctgaaaagt aaataactta acatgttaga 52560atttgcataa agtaaggaaa actggagctg agtacaggac ttgaactgcg ccatctcctc 52620taggccacag aggccttttt gacccccttc caggtcttta gacattgtca ggcagtgagg 52680ggtcgtagct gccagtgtct ccatggtagc gtgctctgcc agggatgcag aagattctcc 52740agtcattcct ccagtgggca cttcctgcag gtcctgtgcc catggctggg agtggtggct 52800gtcattgttc tctgccagaa gggttagcag tgcatcctga cctgacttat gtggcgccca 52860gattcctgga aggggtctaa aaatggacct agacttggtg tagaacgtgt gcctcttggc 52920ctgccaccat ggttccctgc ctggttttgt gtgtcagctc tgccgcttaa gaactgagtg 52980gcttcgggca agttgttctc tctcatagga gtgtgtgaag atgaagcaac ataagctgct 53040tagcccagcg cccagtacct cacgcagaca taagtgctca gtaaatgttg tctgtggtgg 53100ggatggttgt caccaacatc tgaagtgcac ttctaggtca tcaggtgaca tgattggcgc 53160caacacatgg tactcttgat ttagcacatc tcagctgagg cacctcattg atatttgttt 53220aaaaacaaaa acaaaaaacc ttggtgattc tgctgtgaag tcctggccag aaacctccag 53280accgctgatc aacacgcaac agaaccatca ccgttcacct ctttgacatg gtgccaggat 53340accctggatc tctagctttt gctatagttg ctctaattag ggaataatct tgtctttaat 53400attcctttgc tacatttttt aacatttctt atctaaatgg ttttatgaat cagttttaca 53460gagaaaaaaa accagtattt aaaatattct tccaggggct ggtccaagta cagtagtgtt 53520tacaactatg tgatcacaac cagttacaga tttctttgtt ccttctccat ccccactgct 53580ttacttgact agccaaaaaa aaaaaaaaaa aaagttattc cagggaaaca attctccaac 53640tttttcactc ccaatctcac tcctcttatc ttcctcccgt actcctatcc tcctcccgta 53700ctcctatcct cctcccctac tcctatcctc cagtagaaac agtcatttgc tgtgaaggtt 53760atgggggaga atgagtcaag gtagaaggtc acctgctgcc cagctcacag tgctgctggt 53820gatgacagca gtccacagtt acaggcactt gctgaacgag gggctctgta tacacctcag 53880ctcattgact cttcccacaa ccctcttgtc acctaccatt tagcaaatga aaaaaccaag 53940gctctgaggt gagttgtttg cccagagtca cccagtgctg tttgaaccca ctcacataac 54000caaccaatac cattatgtaa tttttgaggt cttttatctc tgtgatccac ttaaaaatta 54060tccaagtatc tttatttgta ctaagcctcc ataatgagaa acagtgttcc agatggtggc 54120tagttttcaa agacatctct ctttggaatt cttctttaga acaaaaagcc ccagaccact 54180tatccccatt catatcccct ttggacctag ggagaaggta ctatttatag gtgatcacct 54240gagtttattg tcccttgtgc tgtgccagaa ataaaggtcc ccacctgctc ttattagctc 54300tactaacagg ataaggaaag tggccctcag agagctactg cttttgtgac aaacaaatga 54360tacaagaaaa aaaaagtggc tttttaattt tagtgacctg gggcaggact tccaaatgaa 54420agtttatttc taaaaactaa aaggtaaatt taatatactt tcagtgtttg ggcttaaatt 54480ctctttcaag tgtctttgtg atatgctctg aattttaaaa atttagaatc attgaagttc 54540attatacttg aactttaaaa aaaaaaaaca aaaacctcgt ataaaggtca aggtatgact 54600tcatgctgct gtgtacttag gtcatttaat cttcaaacca ctggatagag gttaggttga 54660agttcgatct taaatcctac ctactgtagc tcattgtacc agcaacagct gtagggacta 54720ggtggaattc atggtgggtt ttgttccctt ttaaagattg aagccaccat attttctgcc 54780ctctaaaagt ttatgtcagc caggcatggg tggctcacac ttgtaatccc agcactttgg 54840ggaggctgag gtgggtggat cacttgaggc caggagttcg agaccagcct ggccaacatg 54900gtgaaacccc atctctacta aaaatagaaa aattaggtga gcatggtggc ctgcgcctgt 54960aatcccagct actcgggagg ctgaggcagg agaaacattt gaatccggga gatggaggct 55020gcagtgagct gagaacatgc cactgcactc cagcctgggt gacagagtga gactcttgac 55080tcaaaaaaaa aagttatgca tcagagaaca gatcctttga tgccctcctc tgccctgaaa 55140ggtttttggg ggagagtaat aagtatcaca acaagatatg acctgagaac agatttccca 55200gataggacat gatccatgtt ttaatatggc ttactgctgt tgcttcatag tgtgaagctt 55260cagacacttc tgaaaaccct ttcagaaaat cccagtcgcc ccatactgat gactaatctc 55320aactaaaaca gggcttcagc cagtgtgaat gccactaatg ccaccaactc acctttgctt 55380ttctgtaggg tgtgcacctg tatgtacaca ttcagctttt ccgggattaa cctctgagtt 55440ctggtttgtc tttcagttga ccatagtcgg attaaactac atcaagaaga taatgactat 55500atcaacgcta gtttgataaa aatggaagaa gcccaaagga gttacattct tacccaggta 55560agcagattgt ctgaattttc tatttaatgt caatttaaga gtttgagagt gctgttatcc 55620acacctcaaa taaaatctgc cacatccttt agaaggtcag gatttcagca taccaaaaag 55680cagcaaggaa gggggaaaaa tcatccttca aaggttcagt ttggttataa ggaacgctaa 55740tcttttctgg gaagcataag atgacattgc tggaaatgag agcttataga aaacaacatt 55800aaaatgccag agttgcctgt gtggtctgtt ggcagagaca gcagagccat ggctggagga 55860gggtctgtac ctgtgttgct tccagaagta tttgtcgtag agcacttgtg atggcaaatc 55920taagaacgtt agcagtagac caggaatctc tgtccagagc cattcagagt agctcagcat 55980ggttctcatt ctttggccag aagaaaggca tcattggatc atgtgaacaa gcatgaaaaa 56040tgacttaaaa tttctgttgg cttttggcat ctttatggaa acaaaatcct gaaagtggtt 56100taataattga gcctcttgta aaacactcag tggcatgtga ccaaaagggt atctgggaaa 56160gaggataaaa agagtttctt tttaattaat cttctcaagt cttaacttgt tacctgtaag 56220ttggtctaaa aagactgggt ttcttatttt gtttttcatc ataatttttg tttctcattc 56280catgtcagct ttcagtctta tatggcttta ggccacaggg cgattttgaa catttgtaat 56340tttgcttaat aattaggaaa ttaaaattct ggggaagaca gaatgctcta tgaagaaagg 56400ctgctttgag caaggagcta ggtcagggcg cgttcaactg aggcctttct tcactgcctt 56460tttgtcttgt cccagttcct ccccatttat gactaaaatc agcccagatg cttctcgtca 56520tctgggatgc agagcatcag cccagctgtg ttcagtccta tggggccatt gagtaagttc 56580ttggtgcatg gatacagggc aggcctttac caggccctga gcccctggtc ctcccagcac 56640ctctggggta tttaggggag gctgatgggg gagggggttg ataaggcggg agatgtctgg 56700ggatgaggtt gaggcaaaag tgacttcttg aggactttgc tttttggaga agtcaaattt 56760cctacttctt gatttcagcc cttcaactct ggtatggagt caggaagccc tttaaatacc 56820tgttgtcggg tgtatcatgt caagtgttgc attagcaaat gaccatgtat ccttgtgcta 56880ctgtcctgcc taccccgcat cctagcgctt ccttgggaca tgagaagctc tgtctggttt 56940gtgaggtggc actggggatg ttgagaaact gtttacacag tttccctttg ccctggggat 57000ttactaaagg agtcgaggca gcctgacccc aaagcatcac ccctggacac tatgaccgaa 57060acatttcccc agtgcccaaa ccaagaacac ccttcccatt tttttttcag tggtgttcat 57120tatgtaataa tacaagtctc tcttctcatt ttttaaaagt cagaagtaca gaagagcaga 57180gaataatgtc caaggggccc tccttcacct cccccgtgca gtgtcagcta agtgtggtgc 57240gtgtccttgc agatcttagg ggattgtgat ccttcagacc attctaaact ggggtggtgc 57300tgggagttag ggaaggcatg aagggagtag tggagagctg cagtgactgg ggtcttcatg 57360ccagggtgga gaatgcaagg cccaggtggc cagccatgtg ccacgggatt tctggctgcc 57420aagagctgtt tatctgttca ctggggaggg aagagttaaa tgtggtctgc ttttctccga 57480gtcccttcag cacagggagt gctgacttgt cttgttcagg tagtaagttc aagatgagct 57540caggaaagaa agtgagagga cactgagggc tagtggttga gccaagtgtg atgggactta 57600aagggagaag atttaaagaa taaggagctt atgggccggg gacggtggct tacgcctgta 57660atcccagcac tttgggaggc tgaagcaggt ggatcacttg ggtcaggagt tcgaggccag 57720cctggccaac atggtgaaac cccgtctcta ctaaaaatac agaaattagc tgggtgtggt 57780agtgtgcacc tgtaatccca gctacttggg aggctgagac aggagaatcg cttgagccca 57840ggaggcagag gttgcagtga gccaggattg cgcccctgta ctccagcctg ggtgatggag 57900cgagactctg cctcaaaaaa aattaaaaaa aaataaagag gttaggtgaa aatagatgag 57960aatggaaacc atgagaagaa gtgatgctgg ccaaggacat gacaggttct gatgtggagg 58020tgataggcaa tgtctcttcc agccactgct aataattgag acaaactcaa ggcattcata 58080ccctgtgtcc agtaaacatc tgtgcccatt gccaggtgag ctggattgaa atgggccagc 58140tgctcagcag acaccctcat gccccagtga ctctgttccc cttgggccac ctcattgacc

58200atttatgttt ctacatctcc taagtttgtt gggccaagga tggaggctgt ctgccgtcag 58260ggtcctcatt gctgatggta ggaatagttg ctgatgtttc attggatgtt gctgtattct 58320agggactgtg ctaagtactt tatagaaatg aacatacttc attttcacag ttttatgaat 58380agggactatt attagtcaag taagcgatgg ggaaactggg gcagggagcg atgaagtgac 58440ttgcgcaagg tcacaagatg atgtgattgg aaccaagaga agtgttgtgg ttggccacgc 58500ccccacactg cctctcatct gcaccaagga gttttgtccc atagcccaag ggccttgggg 58560acgaatctca gtggaggccc ttagcgggcc tgcctgagcc agaaagcaga atcggcattt 58620ttctgtcctt ggttggccca gccctgaact gagatgcgga aatcgccttt cgctgcctgg 58680tagaaaatgg agctgcagtt actgaccacc aggcagagag aggtgggtcc ctgtcccagc 58740ctcagccacc actctgccta agctgtgggg actgagggcg ctgtcgttag ctgactgcag 58800aaggtgagca cacgctgtag catgttatgt ttcagatgtc acatgttgtg ttattgtgtc 58860tttgcagggc cctttgccta acacatgcgg tcacttttgg gagatggtgt gggagcagaa 58920aagcaggggt gtcgtcatgc tcaacagagt gatggagaaa ggttcggtaa gtctcggctt 58980catttgctgt gtatgtgatc atgcatacca ctccatatag ttaccatttt cgtccagatt 59040tttaaattat ttttcttgcc tttgtatttc ctttacgtag tatttttatt taaaaaaatt 59100aaaacagcag catataaatg catgttggtt gtcaaccagt taatgaagtg aataaaaggg 59160aggaggcgga agaactgcac ggacctcttc gcccccgcct tctcctgtgt ggtgcgtgtg 59220gcgctccgcc cacctgtgct gcctgtgcgg ctctcatcac agtgtggagt tgtgtgtgga 59280gttatggaga cctgctttta tcttgaaaag caagttctta gtgcatcttc atggtgtctg 59340attttttggc tggtgagagt gtggctacct ctgcggagct gtgggagcgg ctgactagat 59400gagatttgcc tccattcagt acctagactc ttgccctgcc acacctcttc ggagtgagca 59460ttgacttcag gatgtgtgtc attctaagtt cctgcaactt ttcaaacacc cctcgggcta 59520gcgtgtggct gcacggtgtc catttgtgca ggccaccact cctcttgcat ctgggtctag 59580ccacctctcc ttcttgactt accatagttc attttgtacc atgctttcag aatgagcttt 59640ctcaaatcca agtctcacca cggttcttcc cagctgaaaa cccttgtgcg gttccctttg 59700cctcacagga taatacatgg tgtggcttac ggaaccctgc aggtctggcc ctaggcccct 59760ggacacagac ctctcaccac tcttggaact ttagccagga caaagttttc tgtttttagt 59820ttcttaccat gttctctggg ccgaggagtc ccagtgccca cgttcatccc acttgcaggc 59880acccctggac ggctgccccc agctccccaa ctgcctgcat tctcccctgc cctcctcact 59940ctgttggaat agctgagaat agccgatttc tgggcagccg gcctcctgtg tagactgtcc 60000tgtgtagact gtcctgtgta gattgtctgt gtagactgtc ctgtgtagat tgtctgtgta 60060gactgtcctg tgtagactgt ccatgtaaac tgtcctgtgt agattgtctg tgtagactgt 60120cctgtgtaga ctgtcctgtg tagattgtct gtgtagactg tctctgtaga ccgtcgtgta 60180tagactgtcc tgtgtagact gtctctgtag accgtcgtgt atagactgtc ctgtgtagac 60240tgtctctgta gaccgtcctg tgtagattgt ctgtgtagac catcctgtgt agaccatccc 60300atttagacca tctgcctgtg caggcgcagg ccagtgttca gcagggccac aggctcctcg 60360gcctccctgc cctcgctgct ccccaacact gccaaccctg ctgcggggtc caggaggaga 60420tgggctgagg atcgtggaga ccagcaggag cgtgtggccc aggagcaggg aactgggtgt 60480ccttgggcct tgccaggtcc aggctcagct aggacacggc tctcacagct gtcctggttg 60540cctccggcca cagaagaagg tgagggctcc agagaggcca cctttccaaa aaaagcacag 60600tcatggccct agaatgtaaa aaatccaagt gttaagaagg aacacatcaa aggaaacttc 60660agcagtgaaa acttgaagca ttaaccacga agcctctgcc tccaccacac acaaagaaac 60720ggctttagtt actcgcagaa agtcttcctc ttaggacagc gcgtgtttaa aatcataggg 60780gtttggtttg ttttgttttg gggttggggt tttttggggg ttttttaccc ttgcctactt 60840tttaaaaaat gaaagtgttt atttgcccaa caataacaga cagggagctt gcctaagtgt 60900tctgttgatg atataatgta tcttgtctta gaaaaaaact ttttcagtga aaggtggttt 60960ttaaattttt tcttccctcc ttagtagctt gattagtaaa atgtgaagtt acaaatgtga 61020agcaaacccc cacccttcac cactagtcag caattttgag taaagaaaca aagcatcagg 61080tgctcacagc acacactgtc ttagagggaa ggggaagcct ggtggcctgt ggaagccttc 61140agcatagctc catctgcagg cttctgaccc tcagcactac tgacacttgg gctggatcat 61200tgtctgctag ggatccgggc agggagtggc tgtgctgggc gctgtaggaa gtttagcagc 61260atctctggcc tctatccacc agatgccagt agcaccccct ccccagatgt ggcagtcaga 61320tgtgtttctg tctagactcc agactttgtc caacgtcccc tggtaggcca aattgccccc 61380ggttgagaac caccgctcta gatggtattg agggttggga attttaaatc aagacattta 61440ttcagaaatt accagatata gtagcatttg cttcttattt atttctttgt tgctaagtgt 61500ttggcaaaac ctctttgctg tgagcacaag gtttgcttta gcaattgttg tcacattaca 61560gcaaggagtg gtgtccagcg ctgtagttat gtatttgagc agtgtccagt gctgtagtta 61620tgtgttccag cctcaccagg ccctgtgctt cattgtctcc cactcaagac tgaccacaaa 61680tggcccacag atccactgtg acaacctttc cctttgggtt actgtggtgg catcgagaac 61740atggctggtt ggctttgctg tagtttactg tgataactgt gccagcagtc cctgctttcc 61800tttgttaagt atcccattcc actggaggat tacttgggcg tgcagattgg catgaaaagc 61860aatgtatggt ttgagattgt taaagtttct ttgggatcaa cattttcaat tctgtatcag 61920cattatccct cccagagggc tggctgggag aaatcatgag aagttacagt atcttatttg 61980ctcagctaat ctaattataa atgatccaca cagcttgtgg taaaaccagc ttttggggag 62040ttttcattta atgcatactt gtcttctgat ttccttcctt caccaaatag tgtaggatgc 62100tccctcttat ttttggcaaa catgcctgtt atcttttggg accctgggct tcctggaaac 62160cagttatgca gaagatgatt gtgtgtgtta gactggggtc atccagatgg ctagagttct 62220cactggttct gtttaaggat tgactttaga cacctcagtg taggctgcac catggcgtaa 62280gggttgggat tgttgtttag aagggggaag taagcaaggt gagtttaatt ggccattgca 62340gaatctcacc cgtatctccc tcctgaaatc ctcactaaag ctgccgtttg ctttcaggtg 62400ctttcatgca caagacactg cattttgtat cacagggtcc atataattca tttttctctc 62460gtacttagtt ctctgtgtta agaattactt acttagttct ctgtgttaat aatttttggc 62520gaaaccaaat tacccgtcac agggttactg tagatgtctt tcataggttt tccaaacacc 62580acttgcccac ttgtttggga aggccccaag gactgtttaa catctgcctt catggtggaa 62640acagcaacta tgagagatgc tagcatgttg gcactgccat gttcctctgg taccagccca 62700agataggact caatttgagg cctggtgaag tactgtgttc taataaaaat ccatctactt 62760ttcatggccg tatatatcaa tgtaataggg taactggaaa tgtgatcttg tgccttttaa 62820aaattttgtg tgtttaaaac aaaaatttct attggaaatg acagagcata gcttgttgct 62880gtagacacct gagagtcctt aaaaataaat attgggttat tgacacttag ttgcatgaca 62940gaattcctca cttgtacagt tccaaagtct tagtctttac ccagattaca gagggttatt 63000aagcattagg tttggttttg aaagtgagtg cttgctgtct ggaggtgagc tttaagactc 63060gtctgccctg cttatgagat gaggaagggt ggcctcttcc tcctgcattt ctgttcttcg 63120cttccttctc tgtctgctca ctctgtggaa tgcccacccc agcacgggtg gggtggaacc 63180tgtcagatca gtctcttgtt tctggggtct tgaggcatta taagatctag ttgttagaag 63240tgtgggatta attcatcttt tcacattctt ctaagttcct gcttttagct gccacaccca 63300ctttggctaa gtgggggtct tgccatgtaa ttagcgcctc catgccaagt ggcagaattg 63360cttcaatggt gacagattgt ccccattcaa gagttcactt ttggcaactc atcattgatc 63420caggaaggtg acatggatga aactggctaa gacttcagac aggcttgtgt ccagactctt 63480gagaaagctc tgttggcttc tggtctggca ctgtgaagtt tgctgtgatg ctggcaccac 63540aacctggtgt ttcctaattt gtttctccca cattttgctt tggttttgtc ttttgggcag 63600cttccagctc cagtagagca ggaccaatag gcatttgtgg ttctatattc accctcctca 63660cgtgcttcct ggctcctcat tgcccccaga tgatgccaca ggtccctggg cctgctgcca 63720gtcgtctgtg atctgggcct ctgctggccc cttctccagc tgctcttttc agcctcttat 63780ttgcagtcac tgcctaggaa atcctagtca tccttcaaaa cctgcctctt gcacagagct 63840ttctctgatc tctcttttct gtaaccttgg ctgacctgaa acatttccct cttctgaatt 63900cctgctgcat gtccgtagca tttccccctc agccctcccc catagtccac cttgtcactg 63960ctgggcacag cagtgtcttc tgacagacag ctggccctga agtggttccc ttcacccaca 64020ccatcctttg ccccagagga ggtattgagt gggtcagtgc acgtgaactg ccagtgtcat 64080ttgccaaaga gctgttgaca cacgctgaca tttcttttgc tgaaaatcat aagggctttg 64140agcttccctc tgtccaggca catggtcagg ctgacccggt agctctgccc ctgctgacct 64200gccatttttg tccacaacag ttatccatga gcagaaacat ttgtgtaact gaggcagaaa 64260cttagttcaa gtaaaatgtc actaaattcg agtcagtttt tgtcttagac cctaaatgaa 64320accaaatttt cataaatttt cttgttttaa agaaaaattt aatgagctac atttaaactg 64380agaacatcag atagtgtctg agattatcaa aatagaacat caaaagtatt tttctgaatg 64440aactgaacca aaccagaatg aaagggcaag ccctggggag cctgtctcca agccttctct 64500gaaagggagt ctgtatttgg tgataactgc tcagcctctc caaagggcct cacctgctgt 64560ctctcccagt tttattttta attgcctgtg agttttctgt gcagggtaag gcacctacat 64620tctatgccag cagcctgatc aggtcctggg taatgtttga aatggctaca cagaggagtt 64680tcaaagcctt ttgttcaatc tggcttcacc tcgtagacgg tgagaaagcg tcagagccct 64740gcaggatccc gttgccacgt ttgaccgggg agccgatggg tttggaagtc tgagccctgt 64800ctgcacaacc tgccccggtc agcagcttcg tgcccccacc cccatctccc catgaggcag 64860gcatctgtgc tgaccatggc ttccatgttc agaaaccccc aggcctttga gttatcatga 64920agcttgtggg atgtgctcca agcctcctgc catagaaaaa ctgccatatt gctcacaata 64980attcactatt atttgtttcc ccagttaaaa tgcgcacaat actggccaca aaaagaagaa 65040aaagagatga tctttgaaga cacaaatttg aaattaacat tgatctctga agatatcaag 65100tcatattata cagtgcgaca gctagaattg gaaaacctta cagtgagtat agcacacact 65160tcagcacttc aggcggctac tggttcacat gcctcttcct ttatcccttg ggtgatatta 65220cctaatgtca gtgttcctgg cttttgtata ccccgagcaa gatgtggttt gggcactgtg 65280gtgagcggag cttacttgtg tacctaccaa gtgcccaggg agggtggagg ccacagtgct 65340ctctctgacc tttaacaaca gttaacacca gttcttaggg aaaggagagt ttcttaccca 65400aaagactggt tcctgcttgt gcagctgcag agggactgga gcggcagcct gcaagtccca 65460gtgaagcatg ctgccttctt tgtggtcctc agtcttcgag tctgaagaga gggaagaagg 65520ggtatagggg ctcactccag tttcatagct agtgaaagtt ttctgggcca ggtcttgggt 65580ttttttgttg tgggaagagt ttataacacc agctacttgc ttggtaaaag ttggtcttgg 65640aacatggcaa ggcattgtgg caagcagcac tgccgctgaa cgcgctgctc ctggggcttt 65700ggaataattc ccctggatcc gtaacttggg ggtgttcatg tcattctggg gaacagtgga 65760gggagtgcgc ggcagcacct gggggcacca gtgaagagtg gccagccacc aacctctaga 65820acctaactgg ggtcgaatcc tggccccacc ttactagctc atcacagtgt ctccgtttcc 65880tcttctgtca aactcaggtt ttgcgagggt tctgggaggt cctatacggg aagggttagc 65940agttaccatg ggtgtgtagc acgggcttta tctgaaggga aggtggagcc gtagggagac 66000catgtggagt ggggctccag ggctgtgtgg gtggggaggg atctgcttct gggttacccc 66060atgcctcccc ttctcaagta ctacttttta atcatcatgg ctcctgccat tcatttcata 66120gttgatgtaa gccaggtgcg gtggctcacg tctttaatcc cagcacttgg ggaggctgag 66180gccaggagga tcactcgagg ccaggagttc aagaccagct tgggcaacat agtgagaccc 66240ccgtctctac aaaaaaacaa aaacagttag tcagacatcg tggtgctccc ctatagtcca 66300gctactcagg aggctgaggc aggaggattg cttgtgcccg ggagttcaag gctgcagtga 66360gctatgcttg caccactgca ctctagcctg ggtgacagag caagaccctg tctcaaaaat 66420aaataaataa aaaaaatagt agaagtaaga tctagaatgt agcacaggtt accaggacgt 66480aggcaagggg ttcgggctgc ctggctcttg aggatggtag cagtgcagct gatgtgagtg 66540ctttctgccc tctggtggtg accgcgccgg agtcaccagc cctgccatag ccctgatggg 66600gcagagggtt ctgagtacgg tggatggagg tgctttctgg aagattctca ggagtaacat 66660gggcagtgtg ttggaatgtg ctagaggatt tatgcagtag ccttttaaaa gaatgctttt 66720tagcatttgc aagcctgaca ttaagagtga cttctgggaa actatttgct tgttgaggga 66780aactgaattt caacagagca gaagagctgt gcgctttttg cttggcagag tgaatacagc 66840cagctcagag gttttgatgt taggatctgt ttgctccaac agactttgtt tttaaaaggc 66900ttttctcagc catagctgtc tgttctagca caaggctgga atgagttcct tgtgaaagag 66960gtgagcaggt gtgagggagg gtgtcagtgg gcggtaaccc acaccttcaa ggattaaagg 67020aaaacttgca tttggcatgc ttgcttctta ttcaatttta aaatacattt taacggccgg 67080gcacggtggc taacacctgt aatcccagca ctttgagggg ctgaggtggg tggttcacga 67140ggccaggggt tcaagaccag cctggccaag atggtgaaac cccatctcta ctaaaaatac 67200aaaaaaaaaa aaaattagcc gggcgtggtg gcgggcacct gtaatcccag ctactcggga 67260ggctgaggca gagaattgct tgaacccagg aggcggaggt tgcattgagc cgagatcatg 67320ccactgcatt ccagcctggg cggcagagca agactctgtc tcaaaataat aataataatt 67380ttttaaaaat acattttaag tccttttctt ccccacctgc ctccacccac caaatagaag 67440aggtatttct tcttctttaa tgtcattaag gttatatgga taccattttc tagagaggaa 67500agaatgatgg aattgcctag tgtgagtcta gcaattatcc taacatacac aaatttctcc 67560ttgttctgtg ccaagatact gtatttaata tttaatgaac attaaatatt atttactagt 67620gtatttaatg gctgaggcag ggttaaatat gtattatttt catcccagca gagttggggg 67680aggtcctagt aactatgcca tgagctctgt gagggtgagg tggtgtcttt gcccccgcct 67740ccctggcaca gtgactggca catgattggc atagtgtgga cattcgtcaa gtgaaggaag 67800gcatcatgag cagatctctg gcctgaatcc ttctgccatc agctgctcgc caggtggccc 67860tggcactggg ccacagggaa actctccagg ctggtatggt tcctgtctgt ggctgtcttc 67920ccgggcccat gttaggagac tttcacttcc agagcccttt ccctctcagg gccttgctta 67980ccaagtgact ggttcccatt tactaggagc tcttaggtca ttgaagatgt tgcgtactcc 68040ccccagtgag ggctgccttt tgatcacagc cgccagaagc ctcaaggaag gagcagagct 68100ggaaacagac gccaggccat tgcttctgtt cctctggggc agacccagcc acggaagaga 68160cattctggga caagggctgg ggtccacctt tcaaacgtgt ctgcagcagg ctctcagcat 68220ggactctctg cctccaaaca tccacctcct catcggaaaa tggatgggag tgcctgcctg 68280gagcagctgg tgggagagcg cagcgccagc acgtaggaca cactcggttc atgggctgat 68340gccgttcgca ttgactgcct cttcagctgg gtgttgagcc acaccttgga gtcaccagtc 68400tttggagacc aagtctgcta cttttttctc taaagtgaca atcctctgaa acctccagat 68460catcttgaag cccccgtctg aaagttgccc agagccagtg cctcacctgc tgttccttgt 68520tcactttttc acgggaggcc ttgcagggct ttatgacaag attttatggg tggctgccca 68580gcatcattgt gactcgtgag acagagagaa accagttgta accatgtaga cagtggaagt 68640gatagggaga aaagaggtga ggggactctt caatccgaag ggaaatgaag tctaagcagg 68700cgcaccctgc aggttcagtg tcaagcccag ggcctggccc cagggtgtgg tatttgttga 68760ctgggtgtgt ggaccctggg agaaagtctg agaatgaatg ttcctcttag aggtagagag 68820tggaaggtga ctctgtgtgt acttggaatt agtgatttct gtacagatga ttcttttaga 68880atcatcatga gtatttttct ctttcagacc caagaaactc gagagatctt acatttccac 68940tataccacat ggcctgactt tggagtccct gaatcaccag cctcattctt gaactttctt 69000ttcaaagtcc gagagtcagg gtcactcagc ccggagcacg ggcccgttgt ggtgcactgc 69060agtgcaggca tcggcaggtc tggaaccttc tgtctggctg atacctgcct cttgctggta 69120aggaggccct cgcgggtgcc ctggggagct cctctacctg ctctgctgtg atgttttttc 69180ctaagtagaa actgaagcgc tcctcttcca aaatacagag actcactgtg ttagtctgtt 69240tttgcgttac taataaaggc gtacctgaga ctcggtaatt tgtaaagaaa agaggtttaa 69300ctggctcccg gttctgcagg ctgtacaagc atggcaccag catctgctcg gctcctgggg 69360aggcctcagg gagcttccag tcatggtgga aggtgaaggg gagcaggagc aagagatggg 69420ggaggtccca gactcttaac cagctctctt gtgaatgcat tgcctcaggg agggcaccaa 69480gcctttcatg agggacctgt ccccctgacc cagacacctc ccacccagcc ccacctccaa 69540cactagggat cacatttcag catgagattg ggaggggaca gacatctaac ggtgttatta 69600acgttgccct tgagaattgg acctggctga cttatatctc ctctctggct ttcagatgga 69660caagaggaaa gacccttctt ccgttgatat caagaaagtg ctgttagaaa tgaggaagtt 69720tcggatgggg ctgatccaga cagccgacca gctgcgcttc tcctacctgg ctgtgatcga 69780aggtgccaaa ttcatcatgg gggactcttc cgtgcaggtc agcattgcct ttgtttgaat 69840ccaggtgtga ccattttaac ttttttgtct ttgaaggagg ctgtcagttg taaaagttca 69900aacaccgtct ggtgtcaggg gaaatagcta cccttcatgt ttaaaatagc tagaaagttg 69960tcaaaatgtt caccatgttg cactttgtgc ctttgaagtg ctcacataga gagcattgat 70020aggaagacga gactttattt tcaaaagatt tcatcttcca agtacatggc tgcagccctg 70080agaggccgag agcccctcgc caagccgtca cctctgctca tgcaaaggga tttcctgaca 70140aaccagccga agtgaacact aataggactt cctcttgctg ctctttcaag gatcagtgga 70200aggagctttc ccacgaggac ctggagcccc cacccgagca tatcccccca cctccccggc 70260cacccaaacg aatcctggag ccacacaatg ggaaatgcag ggagttcttc ccaaatcacc 70320agtgggtgaa ggaagagacc caggaggata aagactgccc catcaaggaa gaaaaaggaa 70380gccccttaaa tgccgcaccc tacggcatcg aaaggtaata tgattgggtc ccagcttgtt 70440ggggtgaggg gaaatgactt tctgttctag aaacacacgc tggtactgaa accctgtgga 70500tgcagcctcc tgttggcaag cagcgcttcc gcatccttgg ggaacagggc gcgtggacca 70560cagccactcc actcctggct gctggaggtc cggtattggg cacagggtgg ccgcaggaca 70620tgagccactt ctgtgggctt ctagtgccac cttgtggtgc ttgttggaat gaggggctcg 70680gagccaccga gtagggtttt tctgcccccc ctgacgacag cgccctcccc caggtttccg 70740gacagtcctg aaatgtgatg tccaggcttg agtgccctca gtccccacag tggtcctttg 70800gggaatgtaa ccttttttat gtggtcttga ttaaatccca ttttacttcc ttgcaggtta 70860acaaccatta ttgagtacct attgatatgt gtggtgtact gagttaacta gaacatgtcc 70920cctggtctgt gttctagacc atcttgctgg gaaaaaggca gacccaaagc atattttggt 70980gggggcccat ggacagtgat gtgatagagg tgtccgctga ggtggtcagg gaaggctgct 71040tgcagtaggt ggccgtgcac ggaaagtttg cagaatgagc aggtgttagt tccagctgga 71100gatgactgcc ggctgtgccc ttggtacctg ctttctggag ggaagtttta agacgtgtgc 71160atacttgacc cagcagttgt atacatggag aaatttactt tgcagcaact ctcaaaacaa 71220gcgtgtaaag atgtgtatag gtagttgtgt ttgttgtggc attgtttgta gtagtgaaaa 71280attagagaca ggccaatgat ataaccaggg acctgatcaa ttatgttctc tcccggtgtt 71340gggatattct gtagctctta aagaatgaga tctgggtgta ctgatgtggc cagacattgc 71400aattgcagta catgagaagg caaatcatac agtagtgtgt acaccagtga gtcctccagc 71460cagataaatc ctcacagtga ccagtcgccc aggcaccttg tgaaccctac cctgggtgtg 71520ggtgctatct gaagtacctg ggggaggggg tgacaagtgg acttcaggct gatgtgggcc 71580ctggcctggc cctccctcca agcagagggg gctggctcgc tggaaggtta acatcatcca 71640actctgtcta cacgtggctt gttttttcct agaattcctg ccacaatagc agcatccttg 71700ccattcattt tctccaaagt gagtaaccca tctctgccct ctgattcctc agcatgagtc 71760aagacactga agttagaagt cgggtcgtgg ggggaagtct tcgaggtgcc caggctgcct 71820ccccagccaa aggggagccg tcactgcccg agaaggacga ggaccatgca ctgagttact 71880ggaagccctt cctggtcaac atgtgcgtgg ctacggtcct cacggccggc gcttacctct 71940gctacagggt atgtttccac tgacagacgc gctggcgaga tgctcgtgtg cagagagcac 72000tggccgctag cccgatggta ggattcagtt ctgtggtgca tctgagccag tctcagaaga 72060aacagatcaa aggtttttaa agtctggaac tgtggaaggg ctaacaagag aattaaggat 72120cgatgcactg gggttttaag gagccctctg gtcccaagaa tataagagtc taatctcagg 72180gccttaacct attcaggagt aagtagagaa aatgccaaat acgtctgttt ctctctctct 72240tttttttttt attcctttgt ttttggaaaa aaatagagtt acaacacatt gttgttttta 72300acctttataa aaagcagctt tttgttattt ctggaacaaa aaaaaacaaa gtaggcactt 72360atgaaacttt ctcataccct taggtgatgt aatcagccat ataatttata tttgatttcc 72420cagggaagga atcccaaact tttacgaatg taaactccct tggagaagag ggttaggacg 72480ctgttgcgct caagcccccc tcagctgtgt gcacactgag ccaggacagg gtctttgagc 72540tttcccacta taagaagaac agcaacaaaa ggccgtctag aaaaacagaa cctgcctctg 72600cttctgctca gggtgtcccc gctgggtttc cattgtcctt tctccattgc tccctcctgt 72660gacagccatc ttgctcatgt accagccctc atcaccccat ccccataaat gggtgtcctc 72720gaggcctctg cctgggggtc agaggtcacc acagggtggc cattggcatg tcaacccgct 72780gttaattcag agaagtgggc tccacctcat tgggagaagt gccatttcag cagaaattca 72840cacgttagac gtgtgttgct gttaagtaag gggaagagag aggactagcc tcagagctct 72900ggccatggaa atgacctcct aagacttttt cgtggtttta aatattttac ctctttccag 72960gtggcatctg agtacatcag atggttttgc aaaatgcaaa caattttttc cttggggatg 73020atttttgggg agagggggct actgtaaaaa ataaaaccaa aacccccttt gctccctcgg 73080aggttgaagt tgccgggggg tgtggccggg gtcatgcatg aggcgacagc tctgcaggtg 73140cgggtctggg ctcatctgaa ctgtttggtt tcattccagt tcctgttcaa cagcaacaca 73200tagcctgacc ctcctccact ccacctccac ccactgtccg cctctgcccg cagagcccac

73260gcccgactag caggcatgcc gcggtaggta agggccgccg gaccgcgtag agagccgggc 73320cccggacgga cgttggttct gcactaaaac ccatcttccc cggatgtgtg tctcacccct 73380catcctttta ctttttgccc cttccacttt gagtaccaaa tccacaagcc attttttgag 73440gagagtgaaa gagagtacca tgctggcggc gcagagggaa ggggcctaca cccgtcttgg 73500ggctcgcccc acccagggct ccctcctgga gcatcccagg cgggcggcac gccaacagcc 73560ccccccttga atctgcaggg agcaactctc cactccatat ttatttaaac aattttttcc 73620ccaaaggcat ccatagtgca ctagcatttt cttgaaccaa taatgtatta aaattttttg 73680atgtcagcct tgcatcaagg gctttatcaa aaagtacaat aataaatcct caggtagtac 73740tgggaatgga aggctttgcc atgggcctgc tgcgtcagac cagtactggg aaggaggacg 73800gttgtaagca gttgttattt agtgatattg tgggtaacgt gagaagatag aacaatgcta 73860taatatataa tgaacacgtg ggtatttaat aagaaacatg atgtgagatt actttgtccc 73920gcttattctc ctccctgtta tctgctagat ctagttctca atcactgctc ccccgtgtgt 73980attagaatgc atgtaaggtc ttcttgtgtc ctgatgaaaa atatgtgctt gaaatgagaa 74040actttgatct ctgcttacta atgtgcccca tgtccaagtc caacctgcct gtgcatgacc 74100tgatcattac atggctgtgg ttcctaagcc tgttgctgaa gtcattgtcg ctcagcaata 74160gggtgcagtt ttccaggaat aggcatttgc ctaattcctg gcatgacact ctagtgactt 74220cctggtgagg cccagcctgt cctggtacag cagggtcttg ctgtaactca gacattccaa 74280gggtatggga agccatattc acacctcacg ctctggacat gatttaggga agcagggaca 74340ccccccgccc cccacctttg ggatcagcct ccgccattcc aagtcaacac tcttcttgag 74400cagaccgtga tttggaagag aggcacctgc tggaaaccac acttcttgaa acagcctggg 74460tgacggtcct ttaggcagcc tgccgccgtc tctgtcccgg ttcaccttgc cgagagaggc 74520gcgtctgccc caccctcaaa ccctgtgggg cctgatggtg ctcacgactc ttcctgcaaa 74580gggaactgaa gacctccaca ttaagtggct ttttaacatg aaaaacacgg cagctgtagc 74640tcccgagcta ctctcttgcc agcattttca cattttgcct ttctcgtggt agaagccagt 74700acagagaaat tctgtggtgg gaacattcga ggtgtcaccc tgcagagcta tggtgaggtg 74760tggataaggc ttaggtgcca ggctgtaagc attctgagct gggcttgttg tttttaagtc 74820ctgtatatgt atgtagtagt ttgggtgtgt atatatagta gcatttcaaa atggacgtac 74880tggtttaacc tcctatcctt ggagagcagc tggctctcca ccttgttaca cattatgtta 74940gagaggtagc gagctgctct gctatatgcc ttaagccaat atttactcat caggtcatta 75000ttttttacaa tggccatgga ataaaccatt tttacaaaaa taaaaacaaa aaaagcaagg 75060tgttttggta taataccttt tcaggtgtgt gtggatacgt ggctgcatga ccgggtgggt 75120gggggggagt gtctcagggt cttctgtgac ctcacagaac tgtcagactg tacagttttc 75180caacttgcca tattcatgat gggtttgcat tttagctgca acaataaaat ttttttctaa 75240agaacatgaa tttggggtgc ttcccatttt tttctttgct taatagagct aaaccaggat 75300gagtaactcc tgtttctttc tatccctgct gatgtgaaac agatgttgtc aatcagctgg 75360ggttagagtt ttccacttct aagaattaac ctcagcatcc ctgcattgcc agcaccctca 75420ggctggagcg ctttccttga ctgtgagctt gttgaacacc ttaggcctca gcccatttcc 75480ttcccaaatt gacgctttgc ctgtgtaggg ccctcagata acttaacaaa cttaccagtg 75540ttgtttgaag aacagtgttt tgagttgtaa tctcaaaacc atatccctta cccaattacc 75600tgtaagacac aatggttacc acatctcagt acgtaaagtc cacttgatat agaattgact 75660tagaaataag acagattagt atagtttttc atttgtgtac aaaattaaac aatgtaaatt 75720ccccccaaag tgattttttt gactttttga agtaattttg gacttgcaaa atgttgccaa 75780aatagtacga agagttcccc agtaccctcg aagtttcctc gactgtttca aagctggctg 75840caggcccagg ctcatgagac tgggaagagg acaggctgtg gtcatgtgga cccacaggg 7589924420DNAArtificial SequenceSynthetic Oligonucleotide 244gcgctcttag ccccgaggcc 2024520DNAArtificial SequenceSynthetic Oligonucleotide 245ccagggcggc tgctgcgcct 2024620DNAArtificial SequenceSynthetic Oligonucleotide 246catctccatg acgggccagg 2024720DNAArtificial SequenceSynthetic Oligonucleotide 247ttttccatct ccatgacggg 2024820DNAArtificial SequenceSynthetic Oligonucleotide 248actccttttc catctccatg 2024920DNAArtificial SequenceSynthetic Oligonucleotide 249ttgtcgatct gctcgaactc 2025020DNAArtificial SequenceSynthetic Oligonucleotide 250gacttgtcga tctgctcgaa 2025120DNAArtificial SequenceSynthetic Oligonucleotide 251gctcccggac ttgtcgatct 2025220DNAArtificial SequenceSynthetic Oligonucleotide 252ccagctcccg gacttgtcga 2025320DNAArtificial SequenceSynthetic Oligonucleotide 253tccactgatc ctgcacggaa 2025420DNAArtificial SequenceSynthetic Oligonucleotide 254ccttccactg atcctgcacg 2025520DNAArtificial SequenceSynthetic Oligonucleotide 255atgcctgcta gtcgggcgtg 2025620DNAArtificial SequenceSynthetic Oligonucleotide 256cgggtgtagg ccccttccct 2025720DNAArtificial SequenceSynthetic Oligonucleotide 257atggagtgga gagttgctcc 2025820DNAArtificial SequenceSynthetic Oligonucleotide 258ttgtactttt tgataaagcc 2025920DNAArtificial SequenceSynthetic Oligonucleotide 259cagtactggt ctgacgcagc 2026020DNAArtificial SequenceSynthetic Oligonucleotide 260tctcacgtta cccacaatat 2026120DNAArtificial SequenceSynthetic Oligonucleotide 261tttcttatta aatacccacg 2026220DNAArtificial SequenceSynthetic Oligonucleotide 262aagtaatctc acatcatgtt 2026320DNAArtificial SequenceSynthetic Oligonucleotide 263ttcagcaaca ggcttaggaa 2026420DNAArtificial SequenceSynthetic Oligonucleotide 264gacaatgact tcagcaacag 2026520DNAArtificial SequenceSynthetic Oligonucleotide 265tgcctattcc tggaaaactg 2026620DNAArtificial SequenceSynthetic Oligonucleotide 266ggaagtcact agagtgtcat 2026720DNAArtificial SequenceSynthetic Oligonucleotide 267ccaggacagg ctgggcctca 2026820DNAArtificial SequenceSynthetic Oligonucleotide 268ctgctgtacc aggacaggct 2026920DNAArtificial SequenceSynthetic Oligonucleotide 269tggaatgtct gagttacagc 2027020DNAArtificial SequenceSynthetic Oligonucleotide 270agagtgttga cttggaatgg 2027120DNAArtificial SequenceSynthetic Oligonucleotide 271gctcaagaag agtgttgact 2027220DNAArtificial SequenceSynthetic Oligonucleotide 272tgcctctctt ccaaatcacg 2027320DNAArtificial SequenceSynthetic Oligonucleotide 273tgtttttcat gttaaaaagc 2027420DNAArtificial SequenceSynthetic Oligonucleotide 274tcccaccaca gaatttctct 2027520DNAArtificial SequenceSynthetic Oligonucleotide 275gctctgcagg gtgacacctc 2027620DNAArtificial SequenceSynthetic Oligonucleotide 276aggaggttaa accagtacgt 2027720DNAArtificial SequenceSynthetic Oligonucleotide 277ggtggagagc cagctgctct 2027820DNAArtificial SequenceSynthetic Oligonucleotide 278tattggctta aggcatatag 2027920DNAArtificial SequenceSynthetic Oligonucleotide 279gacctgatga gtaaatattg 2028020DNAArtificial SequenceSynthetic Oligonucleotide 280ttcttcatgt caaccggcag 2028120DNAArtificial SequenceSynthetic Oligonucleotide 281gccccgaggc ccgctgcaat 2028220DNAArtificial SequenceSynthetic Oligonucleotide 282tagtgaacta ttgttacaac 2028320DNAArtificial SequenceSynthetic Oligonucleotide 283tgctaagcca cttctaatca 2028420DNAArtificial SequenceSynthetic Oligonucleotide 284caggattcta agttattaaa 2028520DNAArtificial SequenceSynthetic Oligonucleotide 285tgggcaggat ggctctggta 2028620DNAArtificial SequenceSynthetic Oligonucleotide 286tacaatacta tctgtgacta 2028720DNAArtificial SequenceSynthetic Oligonucleotide 287gatacttaca gggactgacg 2028820DNAArtificial SequenceSynthetic Oligonucleotide 288aaccctgagg cgaaaggagt 2028920DNAArtificial SequenceSynthetic Oligonucleotide 289ccccaggtca ctaaaattaa 2029020DNAArtificial SequenceSynthetic Oligonucleotide 290aaagcaaagg tgagttggtg 2029120DNAArtificial SequenceSynthetic Oligonucleotide 291gctcaattat taaaccactt 2029220DNAArtificial SequenceSynthetic Oligonucleotide 292agtcctcaag aagtcacttt 2029320DNAArtificial SequenceSynthetic Oligonucleotide 293gaaagcaggg actgctggca 2029420DNAArtificial SequenceSynthetic Oligonucleotide 294aaaactggga gagacagcag 2029520DNAArtificial SequenceSynthetic Oligonucleotide 295acatggaagc catggtcagc 2029620DNAArtificial SequenceSynthetic Oligonucleotide 296attgctagac tcacactagg 2029720DNAArtificial SequenceSynthetic Oligonucleotide 297ggctgtgatc aaaaggcagc 2029820DNAArtificial SequenceSynthetic Oligonucleotide 298cactggctct gggcaacttt 2029920DNAArtificial SequenceSynthetic Oligonucleotide 299gctgggcagc cacccataaa 2030020DNAArtificial SequenceSynthetic Oligonucleotide 300agtcccctca cctcttttct 2030120DNAArtificial SequenceSynthetic Oligonucleotide 301cctccttacc agcaagaggc 2030220DNAArtificial SequenceSynthetic Oligonucleotide 302tgtattttgg aagaggagcg 2030320DNAArtificial SequenceSynthetic Oligonucleotide 303acagactaac acagtgagtc 2030420DNAArtificial SequenceSynthetic Oligonucleotide 304acaaattacc gagtctcagg 2030520DNAArtificial SequenceSynthetic Oligonucleotide 305tcatgaaagg cttggtgccc 2030620DNAArtificial SequenceSynthetic Oligonucleotide 306ttggaagatg aaatcttttg 2030720DNAArtificial SequenceSynthetic Oligonucleotide 307agccatgtac ttggaagatg 2030820DNAArtificial SequenceSynthetic Oligonucleotide 308cgagcccctc attccaacaa 2030920DNAArtificial SequenceSynthetic Oligonucleotide 309cacctcagcg gacacctcta 2031020DNAArtificial SequenceSynthetic Oligonucleotide 310gaaacatacc ctgtagcaga 2031120DNAArtificial SequenceSynthetic Oligonucleotide 311cagagggctc cttaaaaccc 2031220DNAArtificial SequenceSynthetic Oligonucleotide 312attcgtaaaa gtttgggatt 2031320DNAArtificial SequenceSynthetic Oligonucleotide 313ccctcttctc caagggagtt 2031420DNAArtificial SequenceSynthetic Oligonucleotide 314ggaatgaaac caaacagttc 2031520DNAArtificial SequenceSynthetic Oligonucleotide 315aaatggttta ttccatggcc 2031620DNAArtificial SequenceSynthetic Oligonucleotide 316aaaaatttta ttgttgcagc 2031720DNAArtificial SequenceSynthetic Oligonucleotide 317ccggtcatgc agccacgtat 2031820DNAArtificial SequenceSynthetic Oligonucleotide 318gttggaaaac tgtacagtct 2031920DNAArtificial SequenceSynthetic Oligonucleotide 319attttattgt tgcagctaaa 2032020DNAArtificial SequenceSynthetic Oligonucleotide 320cgcctccttc tcggcccact 2032120DNAArtificial SequenceSynthetic Oligonucleotide 321gggcggctgc tgcgcctcct 2032220DNAArtificial SequenceSynthetic Oligonucleotide 322gtggatttgg tactcaaagt 2032320DNAArtificial SequenceSynthetic Oligonucleotide 323aaatggcttg tggatttggt 2032420DNAArtificial SequenceSynthetic Oligonucleotide 324atggtactct ctttcactct 2032520DNAArtificial SequenceSynthetic Oligonucleotide 325gccagcatgg tactctcttt 2032620DNAArtificial SequenceSynthetic Oligonucleotide 326gagagttgct ccctgcagat 2032720DNAArtificial SequenceSynthetic Oligonucleotide 327ggagtggaga gttgctccct 2032820DNAArtificial SequenceSynthetic Oligonucleotide 328ccttgatgca aggctgacat 2032920DNAArtificial SequenceSynthetic Oligonucleotide 329aaagcccttg atgcaaggct 2033020DNAArtificial SequenceSynthetic Oligonucleotide 330agtactacct gaggatttat 2033120DNAArtificial SequenceSynthetic Oligonucleotide 331ttccattccc agtactacct 2033220DNAArtificial SequenceSynthetic Oligonucleotide 332ccatggcaaa gccttccatt 2033320DNAArtificial SequenceSynthetic Oligonucleotide 333caggcccatg gcaaagcctt 2033420DNAArtificial SequenceSynthetic Oligonucleotide 334caactgctta caaccgtcct 2033520DNAArtificial SequenceSynthetic Oligonucleotide 335ccacgtgttc attatatatt 2033620DNAArtificial SequenceSynthetic Oligonucleotide 336ttaaataccc acgtgttcat 2033720DNAArtificial SequenceSynthetic Oligonucleotide 337taagcgggac aaagtaatct 2033820DNAArtificial SequenceSynthetic Oligonucleotide 338cagataacag ggaggagaat 2033920DNAArtificial SequenceSynthetic Oligonucleotide 339gagaactaga tctagcagat 2034020DNAArtificial SequenceSynthetic Oligonucleotide 340agtgattgag aactagatct 2034120DNAArtificial SequenceSynthetic Oligonucleotide 341gacacaagaa gaccttacat 2034220DNAArtificial SequenceSynthetic Oligonucleotide 342ctcatttcaa gcacatattt 2034320DNAArtificial SequenceSynthetic Oligonucleotide 343ggcaggttgg acttggacat 2034420DNAArtificial SequenceSynthetic Oligonucleotide 344aaccacagcc atgtaatgat 2034520DNAArtificial SequenceSynthetic Oligonucleotide 345ttgctgagcg acaatgactt 2034620DNAArtificial SequenceSynthetic Oligonucleotide 346ctggaaaact gcaccctatt 2034720DNAArtificial SequenceSynthetic Oligonucleotide 347gctgggcctc

accaggaagt 2034820DNAArtificial SequenceSynthetic Oligonucleotide 348ttacagcaag accctgctgt 2034920DNAArtificial SequenceSynthetic Oligonucleotide 349acccttggaa tgtctgagtt 2035020DNAArtificial SequenceSynthetic Oligonucleotide 350ttcccatacc cttggaatgt 2035120DNAArtificial SequenceSynthetic Oligonucleotide 351atatggcttc ccataccctt 2035220DNAArtificial SequenceSynthetic Oligonucleotide 352gtgtgaatat ggcttcccat 2035320DNAArtificial SequenceSynthetic Oligonucleotide 353cctgcttccc taaatcatgt 2035420DNAArtificial SequenceSynthetic Oligonucleotide 354gtgtccctgc ttccctaaat 2035520DNAArtificial SequenceSynthetic Oligonucleotide 355cggaggctga tcccaaaggt 2035620DNAArtificial SequenceSynthetic Oligonucleotide 356caggtgcctc tcttccaaat 2035720DNAArtificial SequenceSynthetic Oligonucleotide 357gtggtttcca gcaggtgcct 2035820DNAArtificial SequenceSynthetic Oligonucleotide 358gctgtttcaa gaagtgtggt 2035920DNAArtificial SequenceSynthetic Oligonucleotide 359ggaccgtcac ccaggctgtt 2036020DNAArtificial SequenceSynthetic Oligonucleotide 360caggctgcct aaaggaccgt 2036120DNAArtificial SequenceSynthetic Oligonucleotide 361accatcaggc cccacagggt 2036220DNAArtificial SequenceSynthetic Oligonucleotide 362gttccctttg caggaagagt 2036320DNAArtificial SequenceSynthetic Oligonucleotide 363gtggaggtct tcagttccct 2036420DNAArtificial SequenceSynthetic Oligonucleotide 364ccacttaatg tggaggtctt 2036520DNAArtificial SequenceSynthetic Oligonucleotide 365agctacagct gccgtgtttt 2036620DNAArtificial SequenceSynthetic Oligonucleotide 366ccacgagaaa ggcaaaatgt 2036720DNAArtificial SequenceSynthetic Oligonucleotide 367gaatttctct gtactggctt 2036820DNAArtificial SequenceSynthetic Oligonucleotide 368ccacagaatt tctctgtact 2036920DNAArtificial SequenceSynthetic Oligonucleotide 369gaatgttccc accacagaat 2037020DNAArtificial SequenceSynthetic Oligonucleotide 370gcctggcacc taagccttat 2037120DNAArtificial SequenceSynthetic Oligonucleotide 371atgcttacag cctggcacct 2037220DNAArtificial SequenceSynthetic Oligonucleotide 372ctacatacat atacaggact 2037320DNAArtificial SequenceSynthetic Oligonucleotide 373tttgaaatgc tactatatat 2037420DNAArtificial SequenceSynthetic Oligonucleotide 374ggataggagg ttaaaccagt 2037520DNAArtificial SequenceSynthetic Oligonucleotide 375gccagctgct ctccaaggat 2037620DNAArtificial SequenceSynthetic Oligonucleotide 376ctacctctct aacataatgt 2037720DNAArtificial SequenceSynthetic Oligonucleotide 377gctcgctacc tctctaacat 2037820DNAArtificial SequenceSynthetic Oligonucleotide 378aggcatatag cagagcagct 2037920DNAArtificial SequenceSynthetic Oligonucleotide 379gtcaaccggc agccggaact 2038020DNAArtificial SequenceSynthetic Oligonucleotide 380cctgcagcta ccgccgccct 2038120DNAArtificial SequenceSynthetic Oligonucleotide 381cgctgcaatc cccgacccct 2038220DNAArtificial SequenceSynthetic Oligonucleotide 382accaaaacac cttgcttttt 2038320DNAArtificial SequenceSynthetic Oligonucleotide 383gtattatacc aaaacacctt 2038420DNAArtificial SequenceSynthetic Oligonucleotide 384cacacacctg aaaaggtatt 2038520DNAArtificial SequenceSynthetic Oligonucleotide 385acccggtcat gcagccacgt 2038620DNAArtificial SequenceSynthetic Oligonucleotide 386gtgaggtcac agaagaccct 2038720DNAArtificial SequenceSynthetic Oligonucleotide 387gtacagtctg acagttctgt 2038820DNAArtificial SequenceSynthetic Oligonucleotide 388atggcaagtt ggaaaactgt 2038920DNAArtificial SequenceSynthetic Oligonucleotide 389aatgcaaacc catcatgaat 2039021DNAArtificial SequenceSynthetic Oligonucleotide 390uucaugucgg auauccuggt a 2139121DNAArtificial SequenceSynthetic Oligonucleotide 391ucacuggcuu caugucggat a 2139221DNAArtificial SequenceSynthetic Oligonucleotide 392gguaagaaug uaacuccuut g 2139321DNAArtificial SequenceSynthetic Oligonucleotide 393cuucagagau caauguuaat t 2139421DNAArtificial SequenceSynthetic Oligonucleotide 394uagcugucgc acuguauaat a 2139521DNAArtificial SequenceSynthetic Oligonucleotide 395ccaauucuag cugucgcact g 2139620RNAArtificial SequenceSynthetic Oligonucleotide 396uugauaaagc ccuugaugca 2039720RNAArtificial SequenceSynthetic Oligonucleotide 397ggucaugcac aggcagguug 2039820RNAArtificial SequenceSynthetic Oligonucleotide 398gaagaagggu cuuuccucuu 2039920DNAArtificial SequenceSynthetic Oligonucleotide 399ctgctagcct ctggatttga 2040020DNAArtificial SequenceSynthetic Oligonucleotide 400tagtgcggac ctacccacga 2040121DNAArtificial SequenceSynthetic Oligonucleotide 401gggacgaacu gguguaaugt t 2140221DNAArtificial SequenceSynthetic Oligonucleotide 402cuucuggcau ccgguuuagt t 2140321DNAArtificial SequenceSynthetic Oligonucleotide 403ccaggauauc cgacaugaag c 2140421DNAArtificial SequenceSynthetic Oligonucleotide 404uccgacauga agccagugac t 2140521DNAArtificial SequenceSynthetic Oligonucleotide 405aaggaguuac auucuuaccc a 2140621DNAArtificial SequenceSynthetic Oligonucleotide 406uuaacauuga ucucugaaga t 2140721DNAArtificial SequenceSynthetic Oligonucleotide 407uuauacagug cgacagcuag a 2140821DNAArtificial SequenceSynthetic Oligonucleotide 408gugcgacagc uagaauugga a 2140920RNAArtificial SequenceSynthetic Oligonucleotide 409ugcaucaagg gcuuuaucaa 2041020RNAArtificial SequenceSynthetic Oligonucleotide 410caaccugccu gugcaugacc 2041120RNAArtificial SequenceSynthetic Oligonucleotide 411ucucuugcca gcauuuucac 2041221DNAArtificial SequenceSynthetic Oligonucleotide 412cauuacacca guucguccct t 2141321DNAArtificial SequenceSynthetic Oligonucleotide 413cuaaaccgga ugccagaagt t 2141421DNAArtificial SequenceSynthetic Oligonucleotide 414cgagaggcgg acgggaccgt t 2141521DNAArtificial SequenceSynthetic Oligonucleotide 415cggtcccgtc cgcctctcgt t 21

Claims

What is claimed is:

1. A chimeric antisense oligonucleotide 20 to 50 nucleobases in length targeted to a nucleic acid molecule encoding PTP1B (SEQ ID NO: 3 or 243), wherein said oligonucleotide comprises the sequence selected from the group consisting of SEQ ID NO: 244, 245, 247, 248, 249, 250, 251, 252, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 267, 268, 269, 271, 275, 276, 277, 278, 279, 281, 282, 283, 288, 290, 291, 292, 294, 296, 297, 298, 299, 300, 302, 303, 307, 310, 311, 313, 317, 318, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 340, 342, 347, 349, 350, 352, 353, 354, 355, 356, 357, 360, 361, 362, 363, 364, 365, 366, 368, 369, 371, 372, 374, 377, 378, 380, 381, and 388 wherein said oligonucleotide specifically hybridizes with said nucleic acid molecule encoding PTP and inhibits the expression of human PTP1B.

2. The oligonucleotide of claim 1, which comprises at least one modified internucleoside linkage.

3. The oligonucleotide of claim 2 wherein the modified internucleoside linkage is a phosphorothioate linkage.

4. The oligonucleotide of claim 1, which comprises at least one modified sugar moiety.

5. The oligonucleotide of claim 1, which comprises at least one modified nucleobase.

6. A composition comprising the oligonucleotide of claim 1 and a pharmaceutically acceptable carrier, diluent, enhancer or excipient.

7. A method of inhibiting the expression of PTP1B in cells or tissues comprising contacting said cells or tissues with the oligonucleotide of claim 1 so that expression of PTP1B is inhibited.

8. The oligonucleotide of claim 4, wherein the at least one modified sugar moiety is a 2'-O-methoxyethyl sugar moiety.

9. The oligonucleotide of claim 5, wherein the at least one modified nucleobase is a 5-methylcytosine.

10. The method of claim 7, wherein the cells or tissues are human cells or tissues.

11. A method of treating a disease or condition associated with PTP1B in an animal with the oligonucleotide of claim 1, wherein the disease or condition is selected from a metabolic disease or condition, diabetes, Type 2 diabetes, obesity, and hyperlipidemia.

12. The method of claim 11, wherein the animal is a human.

13. The method of claim 11, wherein the oligonucleotide decreases blood glucose levels in the animal.

14. The method of claim 13, wherein the animal is a diabetic animal.

15. A method of preventing or delaying the onset of a disease or condition associated with PTP1B in an animal with the oligonucleotide of claim 1, wherein the disease or condition is selected from a metabolic disease or condition, diabetes, Type 2 diabetes, obesity, and hyperlipidemia.

16. The method of claim 15, wherein the animal is human.

17. The method of claim 15, wherein treatment with the oligonucleotide prevents or delays the onset of an increase in blood glucose levels in an animal.

18. The method of claim 17, wherein the animal is a diabetic animal.